Prevalence of the LRRK2 G2019S mutation in a UK community based idiopathic Parkinson's disease cohort

The LRRK2 G2019S mutation is the commonest genetic cause of Parkinson's disease (PD) identified to date, although estimates of its prevalence in idiopathic disease vary considerably. Our objectives were to determine G2019S mutation frequency in an unselected, community based cohort of idiopathi...

ver descrição completa

Na minha lista:
Detalhes bibliográficos
Main Authors: Williams‐Gray, C H, Goris, A, Foltynie, T, Brown, J, Maranian, M, Walton, A, Compston, D A S, Sawcer, S J, Barker, R A
Formato: Artigo
Idioma:Inglês
Publicado em: BMJ Group 2006
Assuntos:
Short Report
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2117467/
https://ncbi.nlm.nih.gov/pubmed/16614029
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/jnnp.2005.085019
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!

Registos relacionados