G2019S LRRK2 mutation in French and North African families with Parkinson's disease-Reference-Cited by-同舟云学术

G2019S LRRK2 mutation in French and North African families with Parkinson's disease

Published:2005 Issue:5 Volume:58 Page:784-787
ISSN:0364-5134
Container-title:Annals of Neurology
language:en
Short-container-title:Ann Neurol.

Author:

Lesage Suzanne,Ibanez Pablo,Lohmann Ebba,Pollak Pierre,Tison François,Tazir Myriem,Leutenegger Anne-Louise,Guimaraes Joao,Bonnet Anne-Marie,Agid Yves,Dürr Alexandra,Brice Alexis,

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Reference14 articles.

1. Risk tables for parkinsonism and Parkinson's disease

2. Impact of genetic analysis on Parkinson's disease research

3. Cloning of the Gene Containing Mutations that Cause PARK8-Linked Parkinson's Disease

4. Mutations in LRRK2 Cause Autosomal-Dominant Parkinsonism with Pleomorphic Pathology

5. Roc, a Ras/GTPase domain in complex proteins

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