Genetic and Phenotypic Basis of Autosomal Dominant Parkinson's Disease in a Large Multi-Center Cohort-Reference-Cited by-同舟云学术

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Genetic and Phenotypic Basis of Autosomal Dominant Parkinson's Disease in a Large Multi-Center Cohort

Published:2020-07-28 Issue: Volume:11 Page:
ISSN:1664-2295
Container-title:Frontiers in Neurology
language:
Short-container-title:Front. Neurol.

Author:

Lesage Suzanne,Houot Marion,Mangone Graziella,Tesson Christelle,Bertrand Hélène,Forlani Sylvie,Anheim Mathieu,Brefel-Courbon Christine,Broussolle Emmanuel,Thobois Stéphane,Damier Philippe,Durif Franck,Roze Emmanuel,Tison François,Grabli David,Ory-Magne Fabienne,Degos Bertrand,Viallet François,Cormier-Dequaire Florence,Ouvrard-Hernandez Anne-Marie,Vidailhet Marie,Lohmann Ebba,Singleton Andrew,Corvol Jean-Christophe,Brice Alexis,

Funder

Fondation de France

Association France Parkinson

Fédération pour la Recherche sur le Cerveau

National Institutes of Health

Publisher

Frontiers Media SA

Subject

Clinical Neurology,Neurology

Reference36 articles.

1. The genetic landscape of Parkinson's disease;Lunati;Rev Neurol.,2018

2. Association of LRRK2 exonic variants with susceptibility to Parkinson's disease: a case-control study;Ross;Lancet Neurol.,2011

3. Genotype-phenotype relations for the Parkinson's disease genes SNCA, LRRK2, VPS35: MDSGene systematic review;Trinh;Mov Disord.,2018

4. Parkinson's disease-related LRRK2 G2019S mutation results from independent mutational events in humans;Lesage;Hum Mol Genet.,2010

5. VPS35 mutations in Parkinson disease;Vilariño-Güell;Am J Hum Genet.,2011

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3. Neurocognitive Impairment and Social Cognition in Parkinson’s Disease Patients;Neurology International;2024-04-16

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5. An Overview of the Worldwide Distribution of LRRK2 Mutations in Parkinson’s Disease;Neurodegenerative Disease Management;2023-12

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