Lrrk2 G2385R is an ancestral risk factor for Parkinson's disease in Asia-Reference-Cited by-同舟云学术

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Lrrk2 G2385R is an ancestral risk factor for Parkinson's disease in Asia

Published:2007-03 Issue:2 Volume:13 Page:89-92
ISSN:1353-8020
Container-title:Parkinsonism & Related Disorders
language:en
Short-container-title:Parkinsonism & Related Disorders

Author:

Farrer Matthew J.,Stone Jeremy T.,Lin Chin-Hsien,Dächsel Justus C.,Hulihan Mary M.,Haugarvoll Kristoffer,Ross Owen A.,Wu Ruey-Meei

Publisher

Elsevier BV

Subject

Clinical Neurology,Geriatrics and Gerontology,Neurology

Reference32 articles.

1. Genetics of Parkinson disease: paradigm shifts and future prospects;Farrer;Nat Rev Genet,2006

2. Lrrk2 in Parkinson's disease: protein domains and functional insights;Mata;Trends Neurosci,2006

3. Lrrk2 G2019S as a cause of Parkinson's disease in north African Arabs;Lesage;N Engl J Med,2006

4. Lrrk2 G2019S as a cause of Parkinson's disease in Ashkenazi Jews;Ozelius;N Engl J Med,2006

5. Clinical features of Parkinson disease patients with homozygous leucine-rich repeat kinase 2 G2019S mutations;Ishihara;Arch Neurol,2006

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2. How Parkinson’s Disease-Linked LRRK2 Mutations Affect Different CNS Cell Types;Journal of Parkinson's Disease;2024-06-15

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