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...

Volledige beschrijving

Bewaard in:
Bibliografische gegevens
Hoofdauteurs: 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
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: IOS Press 2009
Onderwerpen:
Other
Online toegang:https://ncbi.nlm.nih.gov/pmc/articles/PMC3835064/
https://ncbi.nlm.nih.gov/pubmed/19822953
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3233/DMA-2009-0641
Tags: Voeg label toe
Geen labels, Wees de eerste die dit record labelt!

Gelijkaardige items