As Frequent as Polyglutamine Spinocerebellar Ataxias: <scp>SCA27B</scp> in a Large German Autosomal Dominant Ataxia Cohort-Reference-Cited by-同舟云学术

As Frequent as Polyglutamine Spinocerebellar Ataxias: SCA27B in a Large German Autosomal Dominant Ataxia Cohort

Published:2023-08 Issue:8 Volume:38 Page:1557-1558
ISSN:0885-3185
Container-title:Movement Disorders
language:en
Short-container-title:Movement Disorders

Author:

Hengel Holger¹²^ORCID,Pellerin David³⁴^ORCID,Wilke Carlo¹²^ORCID,Fleszar Zofia¹²,Brais Bernard⁴,Haack Tobias⁵⁶,Traschütz Andreas¹²^ORCID,Schöls Ludger¹²⁶,Synofzik Matthis¹²^ORCID

Affiliation:

1. Department of Neurology and Hertie‐Institute for Clinical Brain Research University of Tübingen Tübingen Germany

2. German Center of Neurodegenerative Diseases Tübingen Germany

3. Department of Neuromuscular Diseases UCL Queen Square Institute of Neurology and The National Hospital for Neurology and Neurosurgery, University College London London United Kingdom

4. Department of Neurology and Neurosurgery Montreal Neurological Hospital and Institute, McGill University Montreal Quebec Canada

5. Institute of Medical Genetics and Applied Genomics, University of Tübingen Tübingen Germany

6. Centre for Rare Diseases University of Tübingen Tübingen Germany

Funder

Deutsche Forschungsgemeinschaft

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Reference5 articles.

1. Deep Intronic FGF14 GAA Repeat Expansion in Late-Onset Cerebellar Ataxia

2. An intronic GAA repeat expansion in FGF14 causes the autosomal-dominant adult-onset ataxia SCA50/ATX-FGF14