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Clinical features of LRRK2 parkinsonism

✍ Scribed by Kristoffer Haugarvoll; Zbigniew K. Wszolek


Book ID
117754018
Publisher
Elsevier Science
Year
2009
Tongue
English
Weight
113 KB
Volume
15
Category
Article
ISSN
1353-8020

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## Abstract We determined the prevalence of two common leucine‐rich repeat kinase 2 (LRRK2) gene mutations in Australian patients with Parkinson's disease (PD). Of 830 affected patients, eight were heterozygous for the G2019S mutation, and two were heterozygous for the R1441H (4,322 G > A) mutation

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