Predictors of Parkin Mutations in Early Onset Parkinson disease: the CORE-PD Study

BACKGROUND: Mutations in the parkin gene are the most common genetic cause of early-onset Parkinson’s disease (EOPD). Results from a multi-center study of cases with PD systematically sampled by age at onset (AAO) have not been reported. OBJECTIVE: To determine risk factors associated with carrying...

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Autors principals: Marder, K, Tang, M-X, Mejia-Santana, H, Rosado, L, Louis, ED, Comella, C, Colcher, A, Siderowf, A, Jennings, D, Nance, M, Bressman, S, Scott, WK, Tanner, C, Mickel, S, Andrews, H, Waters, C, Fahn, S, Ross, B, Cote, L, Frucht, S, Ford, B, Alcalay, RN, Rezak, M, Novak, K, Friedman, JH, Pfeiffer, R, Marsh, L, Hiner, B, Greg, Neils, Verbitsky, M, Kisselev, S, Caccoppolo, E, Ottman, R, Clark, LN
Format: Artigo
Idioma:Inglês
Publicat: 2010
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Article
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC3329757/
https://ncbi.nlm.nih.gov/pubmed/20558392
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1001/archneurol.2010.95
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