Analysis of Parkinson disease patients from Portugal for mutations in SNCA, PRKN, PINK1 and LRRK2

BACKGROUND: Mutations in the genes PRKN and LRRK2 are the most frequent known genetic lesions among Parkinson's disease patients. We have previously reported that in the Portuguese population the LRRK2 c.6055G > A; p.G2019S mutation has one of the highest frequencies in Europe. METHODS: Here...

ver descrição completa

Na minha lista:
Detalhes bibliográficos
Main Authors: Bras, Jose, Guerreiro, Rita, Ribeiro, Maria, Morgadinho, Ana, Januario, Cristina, Dias, Margarida, Calado, Ana, Semedo, Cristina, Oliveira, Catarina, Hardy, John, Singleton, Andrew
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2008
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2248204/
https://ncbi.nlm.nih.gov/pubmed/18211709
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2377-8-1
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!

Registos relacionados