A Novel SNCA A30G Mutation Causes Familial Parkinsonʼs Disease-Reference-Cited by-同舟云学术

A Novel SNCA A30G Mutation Causes Familial Parkinsonʼs Disease

Published:2021-02-22 Issue:7 Volume:36 Page:1624-1633
ISSN:0885-3185
Container-title:Movement Disorders
language:en
Short-container-title:Mov Disord

Author:

Liu Hui¹^ORCID,Koros Christos²³,Strohäker Timo⁴,Schulte Claudia¹^ORCID,Bozi Maria³,Varvaresos Stefanos²,Ibáñez de Opakua Alain⁴,Simitsi Athina Maria²,Bougea Anastasia²^ORCID,Voumvourakis Konstantinos³,Maniati Matina⁵,Papageorgiou Sokratis G.²³,Hauser Ann‐Kathrin¹,Becker Stefan⁶,Zweckstetter Markus⁴⁶,Stefanis Leonidas²⁵,Gasser Thomas¹

Affiliation:

1. Department for Neurodegenerative Diseases Hertie Institute for Clinical Brain Research, University of Tübingen and German Center of Neurodegenerative Diseases (DZNE) Tübingen Germany

2. 1st Department of Neurology Eginition Hospital, National and Kapodistrian University of Athens Athens Greece

3. 2nd Department of Neurology Attikon Hospital, National and Kapodistrian University of Athens Athens Greece

4. German Center for Neurodegenerative Diseases (DZNE) Göttingen Germany

5. Laboratory of Neurodegenerative Diseases Biomedical Research Foundation of the Academy of Athens Athens Greece

6. Department for NMR‐based Structural Biology Max Planck Institute for Biophysical Chemistry Göttingen Germany

Funder

H2020 European Research Council

Ministry of National Education and Religious Affairs

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/mds.28534

Reference45 articles.

1. Parkinson disease

2. Alpha-Synuclein in Parkinson’s Disease: From Pathogenetic Dysfunction to Potential Clinical Application

3. Mutation in the α-Synuclein Gene Identified in Families with Parkinson's Disease

4. Genetics of Parkinson's Disease

5. A novel -synuclein missense mutation in Parkinson disease

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