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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Bibliografiska uppgifter

Huvudupphov:	Bin eJiao, Ji-feng eGuo, Ya-qin eWang, Xin-xiang eYan, Lin eZhou, Xiao-yan eLiu, Fu-feng eZhang, Ya-fang eZhou, Kun eXia, Bei-sha eTang, Lu eShen
Materialtyp:	Artigo
Språk:	Inglês
Utgiven:	Frontiers Media S.A. 2013-09-01
Serie:	Frontiers in Cellular Neuroscience
Ämnen:	Essential Tremor Parkinson’s disease Alzheimer’s disease C9orf72 risk factor
Länkar:	http://journal.frontiersin.org/Journal/10.3389/fncel.2013.00164/full
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