Association of UBQLN1 mutation with Brown-Vialetto-Van Laere syndrome but not typical ALS

Genetic variants in UBQLN1 gene have been linked to neurodegeneration and mutations in UBQLN2 have recently been identified as a rare cause of amyotrophic lateral sclerosis (ALS). OBJECTIVE: To test if genetic variants in UBQLN1 are involved in ALS. METHODS: 102 and 94 unrelated patients with famili...

ver descrição completa

Na minha lista:
Detalhes bibliográficos
Publicado no:Neurobiol Dis
Main Authors: González-Pérez, Paloma, Lu, Yubing, Chian, Ru-Ju, Sapp, Peter C., Tanzi, Rudolph E., Bertram, Lars, McKenna-Yasek, Diane, Gao, Fen-Biao, Brown, Robert H.
Formato: Artigo
Idioma:Inglês
Publicado em: 2012
Assuntos:
Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4245016/
https://ncbi.nlm.nih.gov/pubmed/22766032
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.nbd.2012.06.018
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!

Registos relacionados