Frequency of known mutations in early onset PD; implication for genetic counseling: the CORE-PD study

OBJECTIVE: To assess the frequency and clinical characteristics of carriers of previously identified mutations in six genes associated with early onset Parkinson disease (EOPD) and provide empirical data that can be used to inform genetic counseling. METHODS: Mutations in SNCA, PRKN, PINK1, DJ1, LRR...

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Detalhes bibliográficos
Main Authors: Alcalay, RN, Caccappolo, E, Mejia-Santana, H, Tang, M-X, Rosado, L, Ross, B, Verbitsky, M, Kisselev, S, Louis, ED, Comella, C, Colcher, A, Jennings, D, Nance, M, Bressman, S, Scott, WK, Tanner, C, Mickel, S, Andrews, H, Waters, C, Fahn, S, Cote, L, Frucht, S, Ford, B, Rezak, M, Novak, K, Friedman, JH, Pfeiffer, R, Marsh, L, Hiner, B, Siderowf, A, Ottman, R, Marder, K, Clark, LN
Formato: Artigo
Idioma:Inglês
Publicado em: 2010
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3329730/
https://ncbi.nlm.nih.gov/pubmed/20837857
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1001/archneurol.2010.194
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