Phenotype in parkinsonian and nonparkinsonian LRRK2 G2019S mutation carriers.

Marras, C; Schüle, B; Schuele, B; Munhoz, R P; Rogaeva, E; Langston, J W; Kasten, M; Meaney, C; Klein, C; Wadia, P M; Lim, S-Y; Chuang, R S-I; Zadikof, C; Steeves, T; Prakash, K M; de Bie, R M A; Adeli, G; Thomsen, T; Johansen, K K; Teive, H A; Asante, A; Reginold, W; Lang, A E

Marras, C; Schüle, B; Schuele, B; Munhoz, R P; Rogaeva, E; Langston, J W; Kasten, M; Meaney, C; Klein, C; Wadia, P M; Lim, S-Y; Chuang, R S-I; Zadikof, C; Steeves, T; Prakash, K M; de Bie, R M A; Adeli, G; Thomsen, T; Johansen, K K; Teive, H A; Asante, A; Reginold, W; Lang, A E.

Affiliation

Marras C; Toronto Western Hospital, Edmond J. Safra Program in Parkinson's Disease, Toronto, ON M5T 2S8 Canada. cmarras@uhnresearch.ca

Neurology ; 77(4): 325-33, 2011 Jul 26.

Article in En | MEDLINE | ID: mdl-21753163

Subject(s)

Genetic Predisposition to Disease; Heterozygote; Mutation; Parkinson Disease/genetics; Phenotype; Protein Serine-Threonine Kinases/genetics; Adult; Aged; Aged, 80 and over; Anxiety/complications; Anxiety/genetics; Color Vision Defects/complications; Color Vision Defects/genetics; Depression/complications; Depression/genetics; Family; Female; Humans; Leucine-Rich Repeat Serine-Threonine Protein Kinase-2; Male; Middle Aged; Neurologic Examination/methods; Olfaction Disorders/complications; Olfaction Disorders/genetics; Parkinson Disease/complications; Psychiatric Status Rating Scales; Tremor/complications; Tremor/genetics

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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Parkinson Disease / Phenotype / Protein Serine-Threonine Kinases / Genetic Predisposition to Disease / Heterozygote / Mutation Type of study: Prognostic_studies / Screening_studies Limits: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Language: En Journal: Neurology Year: 2011 Document type: Article

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