Lrrk2 R1441G-related Parkinson's disease: evidence of a common founding event in the seventh century in Northern Spain

Mutations in the leucine-rich repeat kinase 2 (LRRK2) gene together represent the most common genetic determinant of Parkinson's disease (PD) identified to date. The vast majority of patients with LRRK2-related PD reported in the literature carry one of three pathogenic substitutions: G2019S, R...

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Detalhes bibliográficos
Main Authors: Mata, Ignacio F., Hutter, Carolyn M., González-Fernández, María C., de Pancorbo, Marian M., Lezcano, Elena, Huerta, Cecilia, Blazquez, Marta, Ribacoba, Renee, Guisasola, Luis M., Salvador, Carlos, Gómez-Esteban, Juan C., Zarranz, Juan J., Infante, Jon, Jankovic, Joseph, Deng, Hao, Edwards, Karen L., Alvarez, Victoria, Zabetian, Cyrus P.
Formato: Artigo
Idioma:Inglês
Publicado em: 2009
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2821036/
https://ncbi.nlm.nih.gov/pubmed/19308469
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s10048-009-0187-z
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