Comment to: “<scp>SCA4</scp> Unravelled After More than 25 Years Using Advanced Genomic Technologies”-Reference-Cited by-同舟云学术

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Comment to: “SCA4 Unravelled After More than 25 Years Using Advanced Genomic Technologies”

Published:2024-06 Issue:6 Volume:39 Page:1077-1077
ISSN:0885-3185
Container-title:Movement Disorders
language:en
Short-container-title:Movement Disorders

Author:

Paucar Martin¹²^ORCID,Nilsson Daniel³⁴,Engvall Martin⁵⁶,Laffita‐Mesa José²,Wedell Anna⁵⁶,Svenningsson Per¹²^ORCID

Affiliation:

1. Department of Neurology Karolinska University Hospital Stockholm Sweden

2. Department of Clinical Neuroscience Karolinska Institutet Stockholm Sweden

3. Department of Clinical Genetics and Genomics Karolinska University Hospital Stockholm Sweden

4. Science for Life Laboratory, Department of Molecular Medicine and Surgery Karolinska Institutet Stockholm Sweden

5. Department of Molecular Medicine and Surgery Karolinska Institutet Stockholm Sweden

6. Centre for Inherited Metabolic Diseases Karolinska University Hospital Stockholm Sweden

Publisher

Wiley

Reference8 articles.

1. SCA4 unravelled after more than 25 years using advanced genomic technologies;Rudaks LI;Mov Disord,2024

2. Adaptive long‐read sequencing reveals GGC repeat expansion in ZFHX3 associated with spinocerebellar ataxia type 4;Chen Z;Mov Disord,2024

3. FigueroaK Gross C Buena Atienza Eet al.GGC expansion in ZFHX3 causes SCA4 and impairs autophagy.https://doi.org/10.1101/2023.10.26.23297560

4. Exonic trinucleotide repeat expansions in ZFHX3 cause spinocerebellar ataxia type 4: a poly‐glycine disease;Wallenius J;Am J Hum Genet,2023

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1. Reply to: Comment to “SCA4 Unravelled After More than 25 Years Using Advanced Genomic Technologies”;Movement Disorders;2024-06

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