ANXA11 mutations are associated with amyotrophic lateral sclerosis–frontotemporal dementia

BACKGROUND: The Annexin A11 (ANXA11) gene has been newly identified as a causative gene of amyotrophic lateral sclerosis (ALS) with or without frontotemporal dementia (FTD). The current study aimed to investigate the ANXA11 mutations in a Chinese ALS–FTD or FTD cohort. METHODS: We included ten proba...

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Detalles Bibliográficos
Autores principales: Wang, Yu, Duan, Xiaohui, Zhou, Xiao, Wang, Renbin, Zhang, Xiangfei, Cao, Zhenhua, Wang, Xiaoxia, Zhou, Zhi, Sun, Yu, Peng, Dantao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Neurology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9549789/
https://www.ncbi.nlm.nih.gov/pubmed/36226077
http://dx.doi.org/10.3389/fneur.2022.886887

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9549789/
https://www.ncbi.nlm.nih.gov/pubmed/36226077
http://dx.doi.org/10.3389/fneur.2022.886887

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