Two rare variants of the ANXA11 gene identified in Chinese patients with amyotrophic lateral sclerosis
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DOI: 10.1016/j.neurobiolaging.2018.09.020
Abstract: Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disorder. A recent study has identified mutations in the ANXA11 gene (encoding the calcium-binding protein annexin A11) associated with ALS. Mutation screening of ANXA11 protein-coding exons was… read more here.
Keywords: two rare; amyotrophic lateral; lateral sclerosis; anxa11 gene ... See more keywords