LRRK2 p.G2019S Mutation Is Not Common among Alzheimer’s Disease Patients in Brazil

Mutations in the leucine-rich repeat kinase 2 (LRRK2) gene have emerged as a potential common cause for both sporadic and familial Parkinson’s Disease (PD) in different populations. The pleomorphic features exhibited by LRRK2 mutation carriers and the central role of Lrrk2 protein in the proper func...

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Detalles Bibliográficos
Autores principales: Santos-Rebouças, Cíntia Barros, Abdalla, Cláudia Bueno, Martins, Paloma Águia, Baldi, Fábio José Rodrigues, Santos, Jussara Mendonça, Motta, Luciana Branco, de Borges, Margarete Borges, Souza, Dorotéia Rossi Silva, de Souza Pinhel, Marcela Augusta, Laks, Jerson, Pimentel, Márcia Mattos Gonçalves
Formato: Online Artículo Texto
Lenguaje:English
Publicado: IOS Press 2009
Materias:
Other
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3835064/
https://www.ncbi.nlm.nih.gov/pubmed/19822953
http://dx.doi.org/10.3233/DMA-2009-0641

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