Mutation spectrum of chinese amyotrophic lateral sclerosis patients with frontotemporal dementia

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 investigate...

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Detalles Bibliográficos
Autores principales: Yang, Xunzhe, Sun, Xiaohai, Liu, Qing, Liu, Liyang, Li, Jinyue, Cai, Zhengyi, Zhang, Kang, Liu, Shuangwu, He, Di, Shen, Dongchao, Liu, Mingsheng, Cui, Liying, Zhang, Xue
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9641840/
https://www.ncbi.nlm.nih.gov/pubmed/36345033
http://dx.doi.org/10.1186/s13023-022-02531-2

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