Mutation spectrum of chinese amyotrophic lateral sclerosis patients with frontotemporal dementia

Mutation spectrum of chinese amyotrophic lateral sclerosis patients with frontotemporal dementia

Abstract Background Studies have reported that a noncoding hexanucleotide repeat in C9ORF72, is the most common genetic cause of amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD) among Caucasian population, nevertheless it is rare in Chinese population. Therefore, we aimed to inv...

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Bibliographic Details
Main Authors: Xunzhe Yang, Xiaohai Sun, Qing Liu, Liyang Liu, Jinyue Li, Zhengyi Cai, Kang Zhang, Shuangwu Liu, Di He, Dongchao Shen, Mingsheng Liu, Liying Cui, Xue Zhang
Format: Article
Language:English
Published: BMC 2022-11-01
Series:Orphanet Journal of Rare Diseases
Subjects:
Amyotrophic lateral sclerosis
Frontotemporal dementia
Gene
Variant
Online Access:https://doi.org/10.1186/s13023-022-02531-2

Internet

https://doi.org/10.1186/s13023-022-02531-2

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