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Correction: Comprehensive genetic screening of early-onset dementia patients in an Austrian cohort-suggesting new disease-contributing genes

Human Genomics volume 17, Article number: 79 (2023) Cite this article

The Original Article was published on 17 June 2023

Correction to: Human Genomics (2023) 17:55 https://doi.org/10.1186/s40246-023-00499-z


Following publication of the original article [1], the authors reported an error in Table 1. The correct Table 1 has been provided in this Correction.

Table 1 Basic clinical and genetic characteristics of all 60 EOD patients
Full size table

The original article [1] has been corrected.

Reference

  1. Silvaieh S, König T, Wurm R, et al. Comprehensive genetic screening of early-onset dementia patients in an Austrian cohort-suggesting new disease-contributing genes. Hum Genom. 2023;17:55. https://doi.org/10.1186/s40246-023-00499-z.

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Author notes

  1. Sara Silvaieh and Theresa König have contributed equally to this work.

Authors and Affiliations

  1. Department of Neurology, Medical University of Vienna, Vienna, Austria

    Sara Silvaieh, Theresa König, Raphael Wurm, Tandis Parvizi, Evelyn Berger-Sieczkowski, Stella Goeschl, Christoph Hotzy, Elisabeth Stögmann & Alexander Zimprich

  2. Comprehensive Center for Clinical Neurosciences and Mental Health, Medical University of Vienna, Vienna, Austria

    Sara Silvaieh, Theresa König, Raphael Wurm, Tandis Parvizi, Evelyn Berger-Sieczkowski, Stella Goeschl, Christoph Hotzy, Elisabeth Stögmann & Alexander Zimprich

  3. Institute of Human Genetics, School of Medicine, Technical University of Munich, Munich, Germany

    Matias Wagner & Riccardo Berutti

  4. Institute of Neurogenomics, Helmholtz Centrum, Munich, Germany

    Matias Wagner

  5. Molecular and Clinical Medicine, Ninewells Hospital and Medical School, University of Dundee, Dundee, DD1 9SY, UK

    Esther Sammler

  6. Medical Research Council Protein Phosphorylation and Ubiquitylation Unit, School of Life Sciences, University of Dundee, Dundee, DD1 5EH, UK

    Esther Sammler

Authors
  1. Sara Silvaieh
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  2. Theresa König
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  3. Raphael Wurm
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  4. Tandis Parvizi
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  5. Evelyn Berger-Sieczkowski
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  6. Stella Goeschl
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  7. Christoph Hotzy
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  8. Matias Wagner
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  9. Riccardo Berutti
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  10. Esther Sammler
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  11. Elisabeth Stögmann
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  12. Alexander Zimprich
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Corresponding author

Correspondence to Elisabeth Stögmann.

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Silvaieh, S., König, T., Wurm, R. et al. Correction: Comprehensive genetic screening of early-onset dementia patients in an Austrian cohort-suggesting new disease-contributing genes. Hum Genomics 17, 79 (2023). https://doi.org/10.1186/s40246-023-00525-0

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  • DOI: https://doi.org/10.1186/s40246-023-00525-0

Human Genomics

ISSN: 1479-7364