Parkinson Disease Mutation Database

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Skipper L, Shen H, Chua E, Bonnard C, Kolatkar P, Tan LC, Jamora RD, Puvan K, Puong KY, Zhao Y, Pavanni R, Wong MC, Yuen Y, Farrer M, Liu JJ, Tan EK. Analysis of LRRK2 functional domains in nondominant Parkinson disease. Neurology 65: 1319-21, 2005 (PubMed ID: 16247070)

Mutations

LRRK2: (Arg1067Gln) (IVS33+6T>A)

ID: 58

Zabetian CP, Yamamoto M, Lopez AN, Ujike H, Mata IF, Izumi Y, Kaji R, Maruyama H, Morino H, Oda M, Hutter CM, Edwards KL, Schellenberg GD, Tsuang DW, Yearout D, Larson EB, Kawakami H. LRRK2 mutations and risk variants in Japanese patients with Parkinson's disease. Mov Disord 24: 1034-41, 2009 (PubMed ID: 19343804)

Mutations

LRRK2: (Arg1067Gln) (Pro1446Leu) (Val1450Ile) (Gly2019Ser) (Gly2385Arg)

ID: 182


Mutation color legend:
Red: mutation is pathogenic
Orange: pathogenic nature is unclear
Green: mutation is not pathogenic



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