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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...

Ful tanımlama

Kaydedildi:
Asıl Yazarlar: 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
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: BMC 2022-11-01
Seri Bilgileri:Orphanet Journal of Rare Diseases
Konular:
Amyotrophic lateral sclerosis
Frontotemporal dementia
Gene
Variant
Online Erişim:https://doi.org/10.1186/s13023-022-02531-2
Etiketler: Etiketle
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