C9orf72 mutation is rare in Alzheimer's disease, Parkinson's disease, and essential tremor in China

GGGGCC repeat expansions in the C9orf72 gene have been identified as a major contributing factor in patients with amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD). Given the overlapping of clinical phenotypes and pathological characteristics between these two diseases and Alzhei...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autores principales: Jiao, Bin, Guo, Ji-feng, Wang, Ya-qin, Yan, Xin-xiang, Zhou, Lin, Liu, Xiao-yan, Zhang, Fu-feng, Zhou, Ya-fang, Xia, Kun, Tang, Bei-sha, Shen, Lu
Formato: Artigo
Lenguaje:Inglês
Publicado: Frontiers Media S.A. 2013
Materias:
Neuroscience
Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC3782144/
https://ncbi.nlm.nih.gov/pubmed/24068985
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fncel.2013.00164
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!

Ejemplares similares