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Fig. 1 | Human Genomics

Fig. 1

From: Computational and mitochondrial functional studies of novel compound heterozygous variants in SPATA5 gene support a causal link with epileptogenic encephalopathy

Fig. 1

MRI at 14 months of age (A–E) and at 7 years of age (F–J). Thin corpus callosum was observed on sagital T1 sequence (A, F). Slight bilateral hypomyelination with hypointense T1 signal (B, D, G, I) and hyperintense T2 signal (C, E, H, J) in frontal and occipito-parietal periventricular and deep white matter, was observed

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Human Genomics

ISSN: 1479-7364