Common variation in theLRRK2gene is a risk factor for Parkinson's disease-Reference-Cited by-同舟云学术

Common variation in theLRRK2gene is a risk factor for Parkinson's disease

Published:2012-10-31 Issue:14 Volume:27 Page:1823-1826
ISSN:0885-3185
Container-title:Movement Disorders
language:en
Short-container-title:Mov. Disord.

Author:

Mata Ignacio F.,Checkoway Harvey,Hutter Carolyn M.,Samii Ali,Roberts John W.,Kim Hojoong M.,Agarwal Pinky,Alvarez Victoria,Ribacoba Renee,Pastor Pau,Lorenzo-Betancor Oswaldo,Infante Jon,Sierra María,Gómez-Garre Pilar,Mir Pablo,Ritz Beate,Rhodes Shannon L.,Colcher Amy,Van Deerlin Vivianna,Chung Kathryn A.,Quinn Joseph F.,Yearout Dora,Martinez Erica,Farin Federico M.,Wan Jia Y.,Edwards Karen L.,Zabetian Cyrus P.

Publisher

Wiley

Subject

Clinical Neurology,Neurology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/mds.25226/fullpdf

Reference20 articles.

1. Multiple LRRK2 variants modulate risk of Parkinson disease: a Chinese multicenter study;Tan;Hum Mutat.,2010

2. Quantitative assessment of the effect of LRRK2 exonic variants on the risk of Parkinson's disease: a meta-analysis;Wu;Parkinsonism Relat Disord.,2012

3. LRRK2 mutations and risk variants in Japanese patients with Parkinson's disease;Zabetian;Mov Disord.,2009

4. A common missense variant in the LRRK2 gene, Gly2385Arg, associated with Parkinson's disease risk in Taiwan;Di Fonzo;Neurogenetics.,2006

5. Analysis of Lrrk2 R1628P as a risk factor for Parkinson's disease;Ross;Ann Neurol.,2008

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4. Low Levels of LRRK2 Gene Expression are Associated with LRRK2 SNPs and Contribute to Parkinson’s Disease Progression;NeuroMolecular Medicine;2020-10-04

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