ANXA11 mutations are associated with amyotrophic lateral sclerosis–frontotemporal dementia

ANXA11 mutations are associated with amyotrophic lateral sclerosis–frontotemporal dementia

BackgroundThe 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.MethodsWe included ten probands/p...

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Bibliographic Details
Main Authors: Yu Wang, Xiaohui Duan, Xiao Zhou, Renbin Wang, Xiangfei Zhang, Zhenhua Cao, Xiaoxia Wang, Zhi Zhou, Yu Sun, Dantao Peng
Format: Article
Language:English
Published: Frontiers Media S.A. 2022-09-01
Series:Frontiers in Neurology
Subjects:
annexin A11
ANXA11
amyotrophic lateral sclerosis
frontotemporal dementia
genotype
phenotype [mesh]
Online Access:https://www.frontiersin.org/articles/10.3389/fneur.2022.886887/full

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https://www.frontiersin.org/articles/10.3389/fneur.2022.886887/full

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