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...

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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: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2013
Materias:
Neuroscience
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3782144/
https://www.ncbi.nlm.nih.gov/pubmed/24068985
http://dx.doi.org/10.3389/fncel.2013.00164

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3782144/
https://www.ncbi.nlm.nih.gov/pubmed/24068985
http://dx.doi.org/10.3389/fncel.2013.00164

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