𝔖 Bobbio Scriptorium
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1030 Genetic analysis of LRRK2 mutations in patients with Parkinson's disease

Book ID
123047728
Publisher
Elsevier Science
Year
2005
Tongue
English
Weight
250 KB
Volume
238
Category
Article
ISSN
0022-510X

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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