학술논문
Early-onset parkinsonism associated with PINK1mutations
Document Type
Article
Author
Bonifati, V; Rohé, C F.; Breedveld, G J.; Fabrizio, E; De Mari, M; Tassorelli, C; Tavella, A; Marconi, R; Nicholl, D J.; Chien, H F.; Fincati, E; Abbruzzese, G; Marini, P; De Gaetano, A; Horstink, M W.; Maat-Kievit, J A.; Sampaio, C; Antonini, A; Stocchi, F; Montagna, P; Toni, V; Guidi, M; Libera, A Dalla; Tinazzi, M; De Pandis, F; Fabbrini, G; Goldwurm, S; de Klein, A; Barbosa, E; Lopiano, L; Martignoni, E; Lamberti, P; Vanacore, N; Meco, G; Oostra, B A.
Source
Neurology (Ovid); July 2005, Vol. 65 Issue: 1 p87-95, 9p
Subject
Language
ISSN
00283878; 1526632X
Abstract
To assess the prevalence, nature, and associated phenotypes of PINK1gene mutations in a large series of patients with early-onset (<50 years) parkinsonism.