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A novel SETX gene mutation associated with Juvenile amyotrophic lateral sclerosis

OBJECTS: This study aimed to report a novel point mutation associated with juvenile amyotrophic lateral sclerosis (JALS) in a Chinese Han family. METHODS: Detailed clinical assessment was applied to two patients, including proband (II‐2) and his mother (I‐2). Next‐generation sequencing (NGS), also k...

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Detalhes bibliográficos
Publicado no:Brain Behav
Main Authors: Ma, Limin, Shi, Yingying, Chen, Zhongcan, Li, Shujian, Zhang, Jiewen
Formato: Artigo
Idioma:Inglês
Publicado em: John Wiley and Sons Inc. 2018
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6160657/
https://ncbi.nlm.nih.gov/pubmed/30052327
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/brb3.1066
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