Genetic screening for a single common LRRK2 mutation in familial Parkinson's disease.
Nichols WC; Pankratz N; Hernandez D; Paisán-Ruíz C; Jain S; Halter CA; Michaels VE; Reed T; Rudolph A; Shults CW; Singleton A; Foroud T; Lancet, 2005, vol. 365, issue 9457, p 410, ISSN 1474547x. ISBN 1474547x.

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