Comprehensive analysis ofLRRK2in publicly available Parkinson's disease cases and neurologically normal controls-Reference-Cited by-同舟云学术

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Comprehensive analysis ofLRRK2in publicly available Parkinson's disease cases and neurologically normal controls

Published:2008-01-22 Issue:4 Volume:29 Page:485-490
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Hum. Mutat.

Author:

Paisán-Ruíz Coro,Nath Priti,Washecka Nicole,Gibbs J. Raphael,Singleton Andrew B.

Funder

Intramural Program, National Institute on Aging, National Institutes of Health, Department of Health and Human Services

Neurotoxin Exposure Treatment Research Program (NETRP), Department of Defense

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference28 articles.

1. Haploview: analysis and visualization of LD and haplotype maps;Barrett;Bioinformatics,2005

2. Common variants of LRRK2 are not associated with sporadic Parkinson's disease;Biskup;Ann Neurol,2005

3. G2019S dardarin substitution is a common cause of Parkinson's disease in a Portuguese cohort;Bras;Mov Disord,2005

4. Frequency of LRRK2 mutations in early- and late-onset Parkinson disease;Clark;Neurology,2006

5. A frequent LRRK2 gene mutation associated with autosomal dominant Parkinson's disease;Di Fonzo;Lancet,2005

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