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2. 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 Jan 29-Feb 4; 365(9457):410-2. PubMed ID: 15680455 [TBL] [Abstract][Full Text] [Related]
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7. LRRK2 haplotype-sharing analysis in Parkinson's disease reveals a novel p.S1761R mutation. Lorenzo-Betancor O; Samaranch L; Ezquerra M; Tolosa E; Lorenzo E; Irigoyen J; Gaig C; Pastor MA; Soto-Ortolaza AI; Ross OA; Rodríguez-Oroz MC; Valldeoriola F; Martí MJ; Luquin MR; Perez-Tur J; Burguera JA; Obeso JA; Pastor P Mov Disord; 2012 Jan; 27(1):146-51. PubMed ID: 22038903 [TBL] [Abstract][Full Text] [Related]
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