A hypomorphic inherited pathogenic variant in DDX3X causes male intellectual disability with additional neurodevelopmental and neurodegenerative features
© The Author(s). 2018
Received: 30 November 2017
Accepted: 15 February 2018
Published: 1 March 2018
Intellectual disability (ID) is a common condition with a population prevalence frequency of 1–3% and an enrichment for males, driven in part by the contribution of mutant alleles on the X-chromosome. Among the more than 500 genes associated with ID, DDX3X represents an outlier in sex specificity. Nearly all reported pathogenic variants of DDX3X are de novo, affect mostly females, and appear to be loss of function variants, consistent with the hypothesis that haploinsufficiency at this locus on the X-chromosome is likely to be lethal in males.
We evaluated two male siblings with syndromic features characterized by mild-to-moderate ID and progressive spasticity. Quad-based whole-exome sequencing revealed a maternally inherited missense variant encoding p.R79K in DDX3X in both siblings and no other apparent pathogenic variants. We assessed its possible relevance to their phenotype using an established functional assay for DDX3X activity in zebrafish embryos and found that this allele causes a partial loss of DDX3X function and thus represents a hypomorphic variant.
Our genetic and functional data suggest that partial loss of function of DDX3X can cause syndromic ID. The p.R79K allele affects a region of the protein outside the critical RNA helicase domain, offering a credible explanation for the observed retention of partial function, viability in hemizygous males, and lack of pathology in females. These findings expand the gender spectrum of pathology of this locus and suggest that analysis for DDX3X variants should be considered relevant for both males and females.
Intellectual disability (ID) is a common (estimated prevalence of 1–3% [1–3]), clinically variable phenotype, defined by impairment in both intellectual function and adaptive behavior, with onset during the developmental period [4, 5]. ID is clinically and etiologically heterogeneous, with varying disability of the two aspects of the condition . In addition, ID can occur as an isolated trait but is accompanied frequently by one or more co-morbidities; these can include seizures or other neurological involvement , microcephaly or macrocephaly , dysmorphic features, and structural and/or functional abnormalities in organ systems other than the brain .
ID is more prevalent in males than females with a ratio of 1.3–1.4:1 , a gender bias partially reflective of the observation that numerous genes on the X-chromosome contribute to ID under an X-linked recessive paradigm . Indeed, substantial gene discovery efforts have focused on male-enriched or male-specific cohorts as a means to accelerate the discovery of ID-associated genes and mutational mechanisms . Genetic and genomic studies of individuals, families, and populations with ID have led to the identification of more than 500 mutated genes, with some estimates predicting that number to exceed 1000, possibly reflective of the large number of transcripts expressed in and necessary for the development and maintenance of the central nervous system [10, 11]. In several instances, female carriers are protected by virtue of functional mosaicism due to random X-inactivation or by X-inactivation that favors the wild-type allele . Further phenotypic analyses have also led to the appreciation of subtle phenotypic defects under a dosage model, in which males manifest the extreme range of pathology and females are partially protected .
The DDX3X locus on Xp11.4 represents an exception to the male specificity paradigm. To date, DDX3X pathogenic variants have been reported in 35 females with ID [3, 14], all of which were de novo. As of September 2017, 52 cases have been deposited in Decipher: 49 females, all but one of whom have de novo alleles (the 50th was inherited from a mosaic father) and three males, two harbor de novo mutations and one whose mutation is of unknown origin . Consistent with the intolerance of the locus to variation , there are no null alleles found in control populations of either gender and a concomitant depletion of missense variants as well .
Herein, we report our investigation of two adult male siblings with ID, born to parents of normal intelligence. Whole-exome sequencing (WES) identified a rare, non-synonymous, maternally transmitted variant in DDX3X as a likely driver of their phenotype. DDX3X is necessary for canonical Wnt signaling , an observation utilized previously to develop an in vivo ventralization assay in zebrafish embryos as a means to assess the pathogenic potential of alleles . Using this assay, we found that the DDX3X variant results in reduced DDX3X function, reinforcing the genetic hypothesis. Together, our data support the notion that partial loss of function in DDX3X can lead to ID in males and reinforce a gradient of severity model that is dependent on the strength of the mutation as it pertains to residual protein function.
Materials and methods
We studied a pedigree with two affected male siblings. Diagnostic testing of subjects was done as part of their clinical evaluations with informed consent from the mother and assent of the two cases. Research-based testing protocols were approved by the Cleveland Clinic Institutional Review Board.
WES was carried out at GeneDx, Inc. subsequent to informed consent of the parents and assent of the affected individuals. Using genomic DNA from the ID cases and their parents, the exonic regions and flanking splice junctions of the genome were captured using the Clinical Research Exome kit (Agilent Technologies, Santa Clara, CA). Massively parallel (NextGen) sequencing was done on an Illumina system with 100 bp paired-end reads. The percent coverage at 10X or greater in the two brothers and their two parents ranged from 97.14 to 97.49%; the younger brother had 97.18% coverage that was at least 10X and the older brother had 97.49% coverage at least at 10X. The mean coverage in the younger brother was 132X and in the older brother 197X. The mean coverage in the father and the mother was 134.29X and 222.05X, respectively.
Reads were aligned to human genome build GRCh37/UCSC hg19 and were analyzed for sequence variants using a custom-developed analysis tool. Additional sequencing technology and variant interpretation protocols have been described . The general assertion criteria for variant classification are available on the GeneDx ClinVar submission page (http://www.ncbi.nlm.nih.gov/clinvar/submitters/26957/). Variants of possible clinical significance relative to the phenotype of interest were confirmed by Sanger sequencing. Variants were named according to the following GenBank identifiers: DDX3X (NM_001356) and SPG7 (NM_003119).
In vivo complementation studies in zebrafish
We obtained a plasmid containing the wild-type (wt) human open reading frame (ORF) of DDX3X and WNT3A from Ultimate ORF Collection (LifeTechnologies; clone ID DDX3X: IOH13891; WNT3A: IOH80731). Both plasmids were sequence-confirmed and cloned into the pCS2+ vector using Gateway LR clonase II-mediated recombination (LifeTechnologies) as described . For WNT3A, a stop codon was introduced by site-directed mutagenesis using primer (5′-ctgcaaggccgccaggcacTAGGGTGGGCGCGCCGA-3′ and its reverse complement). To generate the mutant constructs for the ID-associated variant c.236 G>A (p.R79K) along with the positive control female variant c.641T>C (p.I214T) and a negative control male variant c.898G>T (p.V300F), we conducted site-directed mutagenesis using primers (c.641T>C: 5′-CTATTCCTATTACCAAAGAGAAAAG-3′, c.898G>T: 5′CTAGAGTTCGTCCTTGCGTGTTTTATGGTGGTGCCGATATT-3′, and c.236 G>A G: 5′-TTGGATCTCGTAGTGATTCAAAAGGGAAGTCTAGCTTC-3′ and their reverse complements). We then generated capped mRNA from linearized wt-DDX3X and WNT3A pCS2+ constructs as well as for DDX3X variants with the mMessage mMachine SP6 kit (ThermoFisher). Injections were conducted with wt (ZDR) embryos, and resulting embryos were phenotyped at 48 hpf for eye phenotypes according to established criteria (class I: hypoplasia of the eye and class II: absence of one or both eyes; . The mRNAs (wt-WNT3A, wt-DDX3X, and DDX3X variants) were injected in the yolk of the embryos at 1–4 cell stage as described . We acquired lateral and dorsal images with an AZ100 florescent microscope (Nikon), digital sight black and white camera (Nikon), and NIS Elements software (Nikon) at × 4 magnification. We determined statistical differences between pairs of batches with an unpaired t test.
Summary of clinical findings in the two subjects. Human phenotype ontology (HPO) terms and codes are shown
Intellectual disability or related neurodevelopmental disability
Tight heel cords
Progressive spastic paraparesis
Proximal leg weakness
Brain MRI with abnormal periventricular T2 intensity
Atrophy of corpus callosum, esp. the genu and anterior body of corpus callosum
Increased cerebrospinal fluid alanine level
At 14 years of age, he developed a stiff gait. Exam at 15 years showed an acquired macrocephaly, an asymmetric spastic gait, lower extremity hyperreflexia, and tight heel cords. He began treatment with oral baclofen for spasticity at 17 years of age. He had an adjusted curriculum during high school, graduated at 19 years, and has worked part-time afterwards in a supported workplace. His gait slowly worsened and he was last able to ambulate independently at 21 years. On neurological exam at 23 years, there was a slow, spastic gait, decreased lower extremity strength, especially with hip flexion, markedly increased the tone of the lower extremities, lower extremity hyperreflexia, and slowed fine finger and rapid alternating movements. At 29 years of age, he has progressive lower extremity and hand weakness and decreased fine motor function.
Brain MRI scan at 16 years of age (Fig. 1i) showed mildly prominent lateral ventricles and cortical sulci, atrophy of the entire corpus callosum that was accentuated in the anterior body and genu, and mild, symmetric, confluent T2-hyperintensity in the supratentorial periventricular white matter. The follow-up study 2 years later demonstrated further interval enlargement of the lateral ventricles and periventricular white matter T2-hyperintensity, suggesting progression of central white matter volume loss. Myelination was otherwise within normal limits (Fig. 1ii). Cerebrospinal fluid analyses at 19 years showed a normal cell count, CSF glucose, and protein levels and normal CSF IgG synthesis and index. Metabolic testing included increased CSF alanine and intermittent mildly increased urinary lactate (Additional file 2: Table S1).
The younger affected brother, 25 years old, has progressive spastic paraparesis and tremor and learning disability/mixed expressive-receptive language disorder (Fig. 1; Table 1). The first concern about his neurodevelopmental status was when he was about 2 years old and had mildly delayed speech development; he spoke in sentences at 3 years and began speech therapy at that time. He developed an intentional hand tremor at about 6 years that worsened over time. Developmental assessment at 5.6 years showed normal development in all areas except for mild receptive and expressive language delay. Re-evaluation at 6 years showed receptive and expressive language skills at 39 and 16 percentiles, with weaknesses in auditory memory, interpreting directions, and categorizing words. Assessment at 7 years showed verbal, performance, and full-scale IQ scores of 84, 81, and 81, respectively. Academic achievement testing showed basic reading, reading comprehension, mathematics calculation, mathematics reasoning, and written expression at 1, 5, 16, 9, and 23 percentiles, respectively; receptive and expressive language tested at 37 and 16 percentiles. He did not have significant behavioral issues.
Examination at 15 years old, for worsening hand tremors, showed a non-dysmorphic male with lower extremity hyperreflexia and tremor; the gait and motor tone were normal. At 17 years, he was noted to have a mild spastic gait and bilateral Babinski signs. At 18 years, he was noted to have a worsening asymmetric spastic paretic gait and bilateral hip flexor weakness. Schooling involved an adjusted curriculum with training in service occupations, and he graduated from high school at 18 years of age, subsequently working part-time and requiring supports in complex daily living tasks.
His diagnostic evaluation included an abnormal brain MRI scans at 15, 16, and 17 years of age showing mild, diffuse prominence of the cortical sulci suggesting mild cortical volume loss and mild enlargement of the lateral ventricles, generalized volume loss in the corpus callosum that was more prominent in the genu and anterior body, and mild symmetric confluent periventricular T2-hyperintensity within the supratentorial periventricular white matter suggesting central white matter volume loss that was more prominent in the frontal lobes (Fig. 1iv–vi). There was also slight further enlargement of the lateral ventricles without significant change in the T2-hyperintensity or the corpus callosum over the 2-year period. The MRI of the entire spinal cord was normal in caliber and signal intensity. CSF analyses showed normal cellular CSF and normal levels of CSF glucose and protein, normal CSF IgG synthesis and IgG index, normal levels of CSF lactate and pyruvate, and increased CSF alanine. Plasma amino acid analyses consistently showed mildly moderately increased levels of alanine and, sometimes, increased levels of proline and glycine (Additional file 2: Table S1).
Here, we describe the clinical phenotypes of two adult males who have a rare, maternally inherited missense allele of DDX3X, a major ID locus that to date has been associated with pathology almost exclusively in females. Both genetics and functional testing support a partial loss of function disease transmission. This notion is consistent with the observation that the mother who transmitted the p.R79K is asymptomatic and that the two affected males have significant neurodevelopmental pathology but have survived. Although the formal possibility remains that the mother might exhibit sub-clinical neuroanatomical findings, careful re-examination revealed no overt neurological concerns. In addition to this notion, it would be important to identify the genotype for the maternal uncle and maternal grandfather, but DNA samples from the individuals were not available. This hypothesis is also supported by recent work in the mouse revealing essential roles of Ddx3x in placentation and embryogenesis and the differential phenotypic impacts of inheriting a paternal vs. maternal null allele . Non-lethality of the p.R79K variant in our cases may be due to the maternal, as opposed to paternal, inheritance of the variant. Non-lethality of the p.R79K variant might also be because the location of the amino acid substitution is outside of the critical RNA helicase domain. The DDX3X protein has been investigated extensively , but the region of the protein surrounding amino acid residue 79 has only been studied sparingly, although site-directed mutagenesis of several nearby residues resulted in functional impacts [27, 28]. Finally, non-lethality of the p.R79K variant might be explained on the basis of the expected moderate biophysical impact on the structure of DDX3X consequent to the conservative nature of an arginine to lysine substitution.
There is substantial clinical and neuroradiologic overlap between the phenotype in our two cases and those of the females and few males described to date. The most common traits described thus far include ID, microcephaly, hypotonia, movement disorder and/or spasticity, ventricular enlargement, and hypoplasia of the corpus callosum; the subjects reported here have ID, spasticity, ventricular enlargement, and an attenuated corpus callosum. Our two cases also present with features that are distinct from those of other cases with variants in DDX3X reported to date; these include progressive spasticity with loss of independent ambulation and, consistent with their clinical courses, evidence of a progressive brain central white matter process including atrophy of the corpus callosum, not hypoplasia. Long-term follow-up of the previously reported cases, some of whom were young children, will be important to determine if any of the neurological findings or developmental disabilities are progressive and if there are ongoing brain white matter changes.
It is also possible that a second clinical process that is distinct from DDX3X may be present in the two subjects reported here. In this regard, both subjects have macrocephaly, as does their father and one sister although the father and the subjects’ siblings have clinical phenotypes that are otherwise disparate from the clinical findings in the cases with ID. The finding of increased levels of CSF alanine in both cases and of increased plasma alanine in one case and increased urinary lactate in the other is notable and suggests a disturbance of mitochondrial bioenergetics. No evidence of a primary mitochondrial cytopathy was found, despite considerable investigation, and the relationship of these results to the variant of DDX3X is uncertain. In addition, the existence of a clinical process that is/was present in only one of the subjects is likely in view of the variability in neurodevelopmental phenotype between the subjects, although the basis of this process is unknown. Given the reported spasticity in this pedigree, we did evaluate known spastic paraplegia genes for candidate pathogenic variants. We detected a maternally inherited heterozygous variant in SPG7 in one of the subjects that has been reported to be pathogenic in patients with recessive spastic paraplegia . Although this allele is by itself unable to explain the observed spasticity in our patient, it is possible that it contributes to the phenotype, possibly in epistasis with DDX3X; the same might be true for some of the other ultra-rare alleles discovered in this family (Additional file 3: Table S2). For example, it is intriguing that the older brother with the more extensive pathology is also hemizygous for candidate pathogenic variant in ARGHGAP4, a gene whose product is required for neuronal migration and which has been reported to be mutated in some patients with ID [30–32]. However, both formal functional testing and delineation of additional patients will be necessary to test this hypothesis.
Overall, our findings suggest that mutational analysis of DDX3X in either genetic testing panels or by whole-exome/genome sequencing should not be limited, by testing or interpretation of data, to females. The severity of most discovered DDX3X alleles remains consistent with a model of total haploinsufficiency incompatible with life in males. Further studies in expanded cohorts will illuminate this proposed phenotype-genotype correlation further.
We thank the family for the participation and encouragement of this work. We thank Erica Davis for the critical evaluation of the manuscript and data.
NK is a Brumley Distinguished Professor of Pediatrics. The study was supported by Core Funding from the Center for Human Disease Modeling at Duke University.
Availability of data and materials
All material on this paper is available for distribution subject to appropriate regulatory clearance.
GK and KK performed experiments, reviewed and compiled data, and co-wrote the paper. SMB and ICT and NK reviewed and interpreted the data and provided guidance to the work. MRN assessed the family, reviewed and interpreted the WES data, and co-wrote the manuscript. FMZ reviewed and interpreted WES. PR reviewed the brain MRIs. All authors reviewed and commented on the manuscript. All authors read and approved the final manuscript.
Ethics approval and consent to participate
The study was approved by Cleveland Clinic Institutional Review Board protocol #06-333 review board, and the family was enrolled in the study under informed consent, including consent to publish the study’s findings. All experiments involving the use of zebrafish (Danio rerio) were approved by the Duke University Institutional Animal Care and Use Committee (IACUC).
Consent for publication
Written informed consent for publication of clinical details and clinical images was obtained from the parent of the probands.
NK is a paid consultant and holds founding stock in Rescindo Therapeutics.
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
- Wolfe K, Stueber K, McQuillin A, Jichi F, Patch C, Flinter F, Strydom A, Bass N. Genetic testing in intellectual disability psychiatry: opinions and practices of UK child and intellectual disability psychiatrists. J Appl Res Intellect Disabil. 2017;31(2):273-84.Google Scholar
- van Bokhoven H. Genetic and epigenetic networks in intellectual disabilities. Annu Rev Genet. 2011;45:81–104.View ArticlePubMedGoogle Scholar
- Snijders Blok L, Madsen E, Juusola J, Gilissen C, Baralle D, Reijnders MR, Venselaar H, Helsmoortel C, Cho MT, Hoischen A, et al. Mutations in DDX3X are a common cause of unexplained intellectual disability with gender-specific effects on Wnt signaling. Am J Hum Genet. 2015;97(2):343–52.View ArticlePubMedPubMed CentralGoogle Scholar
- Harris JC. Intellectual disability: Understanding its development, causes, classification, evaluation, and treatment. New York: Oxford University Press; 2006.Google Scholar
- Tasse MJ, Luckasson R, Nygren M. AAIDD proposed recommendations for ICD-11 and the condition previously known as mental retardation. Intellect Dev Disabil. 2013;51(2):127–31.View ArticlePubMedGoogle Scholar
- American Psychiatric Association. Diagnostic and statistical manual of mental disorders : DSM-5: Fifth edition. Arlington: American Psychiatric Publishing; 2013. Google Scholar
- McGrother CW, Bhaumik S, Thorp CF, Hauck A, Branford D, Watson JM. Epilepsy in adults with intellectual disabilities: prevalence, associations and service implications. Seizure. 2006;15(6):376–86.View ArticlePubMedGoogle Scholar
- de Ligt J, Willemsen MH, van Bon BW, Kleefstra T, Yntema HG, Kroes T, Vulto-van Silfhout AT, Koolen DA, de Vries P, Gilissen C, et al. Diagnostic exome sequencing in persons with severe intellectual disability. N Engl J Med. 2012;367(20):1921–9.View ArticlePubMedGoogle Scholar
- Matson JL, Cervantes PE. Comorbidity among persons with intellectual disabilities. Res Autism Spectr Disord. 2013;7(11):1318–22.View ArticleGoogle Scholar
- Vissers LE, Gilissen C, Veltman JA. Genetic studies in intellectual disability and related disorders. Nat Rev Genet. 2016;17(1):9–18.View ArticlePubMedGoogle Scholar
- Kochinke K, Zweier C, Nijhof B, Fenckova M, Cizek P, Honti F, Keerthikumar S, Oortveld MA, Kleefstra T, Kramer JM, et al. Systematic phenomics analysis deconvolutes genes mutated in intellectual disability into biologically coherent modules. Am J Hum Genet. 2016;98(1):149–64.View ArticlePubMedPubMed CentralGoogle Scholar
- Cotton AM, Price EM, Jones MJ, Balaton BP, Kobor MS, Brown CJ. Landscape of DNA methylation on the X chromosome reflects CpG density, functional chromatin state and X-chromosome inactivation. Hum Mol Genet. 2015;24(6):1528–39.View ArticlePubMedGoogle Scholar
- Fieremans N, Van Esch H, Holvoet M, Van Goethem G, Devriendt K, Rosello M, Mayo S, Martinez F, Jhangiani S, Muzny DM, et al. Identification of intellectual disability genes in female patients with a skewed X-inactivation pattern. Hum Mutat. 2016;37(8):804–11.View ArticlePubMedPubMed CentralGoogle Scholar
- Dikow N, Granzow M, Graul-Neumann LM, Karch S, Hinderhofer K, Paramasivam N, Behl LJ, Kaufmann L, Fischer C, Evers C, et al. DDX3X mutations in two girls with a phenotype overlapping Toriello-Carey syndrome. Am J Med Genet A. 2017;173(5):1369–73.View ArticlePubMedGoogle Scholar
- Firth HV, Richards SM, Bevan AP, Clayton S, Corpas M, Rajan D, Vooren SV, Moreau Y, Pettett RM, Carter NP. DECIPHER: database of chromosomal imbalance and phenotype in humans using ensembl resources. Am J Hum Genet. 2009;84(4):524–33.View ArticlePubMedPubMed CentralGoogle Scholar
- Lek M, Karczewski KJ, Minikel EV, Samocha KE, Banks E, Fennell T, O’Donnell-Luria AH, Ware JS, Hill AJ, Cummings BB, et al. Analysis of protein-coding genetic variation in 60,706 humans. Nature. 2016;536:285.View ArticlePubMedPubMed CentralGoogle Scholar
- Cruciat CM, Dolde C, de Groot RE, Ohkawara B, Reinhard C, Korswagen HC, Niehrs C. RNA helicase DDX3 is a regulatory subunit of casein kinase 1 in Wnt-beta-catenin signaling. Science. 2013;339(6126):1436–41.View ArticlePubMedGoogle Scholar
- Tanaka AJ, Cho MT, Millan F, Juusola J, Retterer K, Joshi C, Niyazov D, Garnica A, Gratz E, Deardorff M, et al. Mutations in SPATA5 are associated with microcephaly, intellectual disability, seizures, and hearing loss. Am J Hum Genet. 2015;97(3):457–64.View ArticlePubMedPubMed CentralGoogle Scholar
- Niederriter AR, Davis EE, Golzio C, Oh EC, Tsai IC, Katsanis N. In vivo modeling of the morbid human genome using Danio rerio. J Vis Exp. 2013;78:e50338.Google Scholar
- Davis EE, Frangakis S, Katsanis N. Interpreting human genetic variation with in vivo zebrafish assays. Biochim Biophys Acta. 2014;1842(10):1960–70.View ArticlePubMedPubMed CentralGoogle Scholar
- Adzhubei IA, Schmidt S, Peshkin L, Ramensky VE, Gerasimova A, Bork P, Kondrashov AS, Sunyaev SR: A method and server for predicting damaging missense mutations. In: Nat Methods. 2010;7:248–9.Google Scholar
- Schwarz JM, Cooper DN, Schuelke M, Seelow D. MutationTaster2: mutation prediction for the deep-sequencing age. Nat Methods. 2014;11:361.View ArticlePubMedGoogle Scholar
- Li M, Gong L, Zhao D, Zhou J, Xiang H. The spacer size of I-B CRISPR is modulated by the terminal sequence of the protospacer. Nucleic Acids Res. 2017;45(8):4642–54.View ArticlePubMedPubMed CentralGoogle Scholar
- Liu YP, Tsai IC, Morleo M, Oh EC, Leitch CC, Massa F, Lee BH, Parker DS, Finley D, Zaghloul NA, et al. Ciliopathy proteins regulate paracrine signaling by modulating proteasomal degradation of mediators. J Clin Invest. 2014;124(5):2059–70.View ArticlePubMedPubMed CentralGoogle Scholar
- Chen C-Y, Chan C-H, Chen C-M, Tsai Y-S, Tsai T-Y, Wu Lee Y-H, You L-R. Targeted inactivation of murine Ddx3x: essential roles of Ddx3x in placentation and embryogenesis. Hum Mol Genet. 2016;25(14):2905–22.PubMedGoogle Scholar
- Sharma D, Jankowsky E. The Ded1/DDX3 subfamily of DEAD-box RNA helicases. Crit Rev Biochem Mol Biol. 2014;49(4):343–60.View ArticlePubMedGoogle Scholar
- Gu L, Fullam A, Brennan R, Schroder M. Human DEAD box helicase 3 couples IkappaB kinase epsilon to interferon regulatory factor 3 activation. Mol Cell Biol. 2013;33(10):2004–15.View ArticlePubMedPubMed CentralGoogle Scholar
- Oda S, Schroder M, Khan AR. Structural basis for targeting of human RNA helicase DDX3 by poxvirus protein K7. Structure. 2009;17(11):1528–37.View ArticlePubMedGoogle Scholar
- Elleuch N, Depienne C, Benomar A, Hernandez AM, Ferrer X, Fontaine B, Grid D, Tallaksen CM, Zemmouri R, Stevanin G, et al. Mutation analysis of the paraplegin gene (SPG7) in patients with hereditary spastic paraplegia. Neurology. 2006;66(5):654–9.View ArticlePubMedGoogle Scholar
- Vogt DL, Gray CD, Young WS 3rd, Orellana SA, Malouf AT. ARHGAP4 is anovel RhoGAP that mediates inhibiotion of cell motility and axonal outgrowth. Mol Cell Neurosci. 2007;36(3):332–42.View ArticlePubMedPubMed CentralGoogle Scholar
- Liu F, Guo H, Ou M, Hou X, Sun G, Gong W, Jing H, Tan Q, Xue W, Dai Y, Sui W. ARHGAP4 mutated in a Chinese intellectually challenged family. Gene. 2016;578(2):205–9.View ArticlePubMedGoogle Scholar
- Huang L, Poke G, Gecz J, Gibson K. A novel contiguous gene deletion of AVPR2 and ARHGAP4 genes in male dizygotic twins with nephrogenic diabetes insipidus and intellectual disability. Am J Med Genet A. 2012;158a(10):2511–8.View ArticlePubMedGoogle Scholar