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Genetic analysis of LRRK2 mutations in patients with Parkinson disease

✍ Scribed by Hao Deng; WeiDong Le; Yi Guo; Christine B. Hunter; WenJie Xie; MaoSheng Huang; Joseph Jankovic

Book ID: 119302112
Publisher: Elsevier Science
Year: 2006
Tongue: English
Weight: 237 KB
Volume: 251
Category: Article
ISSN: 0022-510X
DOI: 10.1016/j.jns.2006.09.017

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## Abstract Mutations in the leucine‐rich repeat kinase 2 (__LRRK2__) gene are the most common genetic determinant of Parkinson's disease (PD) in European‐derived populations, but far less is known about __LRRK2__ mutations and susceptibility alleles in Asians. To address this issue, we sequenced t