Analysis of FUS gene mutation in familial amyotrophic lateral sclerosis within an Italian cohort

OBJECTIVE: Mutations in the FUS gene on chromosome 16 have been recently discovered as a cause of familial amyotrophic lateral sclerosis (FALS). This study determined the frequency and identities of FUS gene mutations in a cohort of Italian patients with FALS. METHODS: We screened all 15 coding exon...

ver descrição completa

Na minha lista:
Detalhes bibliográficos
Main Authors: Ticozzi, N, Silani, V, LeClerc, A L., Keagle, P, Gellera, C, Ratti, A, Taroni, F, Kwiatkowski, T J., McKenna-Yasek, D M., Sapp, P C., Brown, R H., Landers, J E.
Formato: Artigo
Idioma:Inglês
Publicado em: American Academy of Neurology 2009
Assuntos:
Articles
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2764725/
https://ncbi.nlm.nih.gov/pubmed/19741215
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1212/WNL.0b013e3181bbff05
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!

Registos relacionados