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Variants in the LRRK1 gene and susceptibility to Parkinson's disease in Norway

✍ Scribed by Kristoffer Haugarvoll; Mathias Toft; Owen A. Ross; Linda R. White; Jan O. Aasly; Matthew J. Farrer


Book ID
116769421
Publisher
Elsevier Science
Year
2007
Tongue
English
Weight
102 KB
Volume
416
Category
Article
ISSN
0304-3940

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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