Genotype–Phenotype Correlations for <scp> ATX‐ <i>TBP</i> </scp> ( <scp>SCA17</scp> ): <scp>MDSGene</scp> Systematic Review-Reference-Cited by-同舟云学术

Genotype–Phenotype Correlations for ATX‐ TBP ( SCA17 ): MDSGene Systematic Review

Published:2022-11-14 Issue:3 Volume:38 Page:368-377
ISSN:0885-3185
Container-title:Movement Disorders
language:en
Short-container-title:Movement Disorders

Author:

Rossi Malco¹²^ORCID,Hamed Moath³,Rodríguez‐Antigüedad Jon⁴⁵^ORCID,Cornejo‐Olivas Mario⁶⁷^ORCID,Breza Marianthi⁸⁹^ORCID,Lohmann Katja¹⁰^ORCID,Klein Christine¹⁰,Rajalingam Rajasumi¹¹,Marras Connie¹¹,van de Warrenburg Bart P.¹²

Affiliation:

1. Sección de Movimientos Anormales, Departamento de Neurología Fleni Buenos Aires Argentina

2. Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET) Buenos Aires Argentina

3. New York‐Presbyterian Brooklyn Methodist Hospital Brooklyn New York USA

4. Movement Disorders Unit, Neurology Department Sant Pau Hospital Barcelona Spain

5. Institut d'Investigacions Biomediques‐Sant Pau Barcelona Spain

6. Neurogenetics Research Center Instituto Nacional de Ciencias Neurológicas Lima Peru

7. Carrera de Medicina Universidad Científica del Sur Lima Peru

8. 1st Department of Neurology, School of Medicine Eginition Hospital, National and Kapodistrian University of Athens Athens Greece

9. Department of Neuromuscular Disease UCL Queen Square Institute of Neurology, The National Hospital for Neurology and Neurosurgery London UK

10. Institute of Neurogenetics University of Lübeck Lübeck Germany

11. Edmond J. Safra Program in Parkinson's Disease Morton and Gloria Shulman Movement Disorders Clinic, Toronto Western Hospital, UHN Toronto Ontario Canada

12. Department of Neurology Donders Institute for Brain, Cognition & Behaviour, Radboud University Medical Center Nijmegen the Netherlands

Funder

International Parkinson and Movement Disorder Society

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/mds.29278

Reference75 articles.

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2. A neurological disease caused by an expanded CAG trinucleotide repeat in the TATA-binding protein gene: a new polyglutamine disease? [In Process Citation]

3. Different types of repeat expansion in the TATA-binding protein gene are associated with a new form of inherited ataxia

4. Clinical features and neuropathology of autosomal dominant spinocerebellar ataxia (SCA17)

5. Movement disorders in spinocerebellar ataxias

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