No Evidence for Pathogenic Role of UBQLN2 Mutations in Sporadic Amyotrophic Lateral Sclerosis in the Mainland Chinese Population

Mutations in the UBQLN2 gene, which encodes a member of the ubiquitin-like protein family (ubiquilin-2), have been identified in patients with dominant X-linked amyotrophic lateral sclerosis (ALS) and ALS with frontotemporal dementia (FTD). We analyzed mutations in the UBQLN2 gene in a Chinese cohor...

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Detalles Bibliográficos
Autores principales: Huang, Xiao, Shen, Shen, Fan, Dongsheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5268382/
https://www.ncbi.nlm.nih.gov/pubmed/28125704
http://dx.doi.org/10.1371/journal.pone.0170943

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5268382/
https://www.ncbi.nlm.nih.gov/pubmed/28125704
http://dx.doi.org/10.1371/journal.pone.0170943

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