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LRRK2 mutations in Basque patients with Parkinson's disease – Authors' reply

✍ Scribed by Daniel G Healy

Book ID
114409027
Publisher
The Lancet
Year
2008
Tongue
English
Weight
46 KB
Volume
7
Category
Article
ISSN
1474-4465

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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