Genetic screening of ANXA11 revealed novel mutations linked to amyotrophic lateral sclerosis
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DOI: 10.1016/j.neurobiolaging.2020.10.015
Abstract: ANXA11 mutations have previously been discovered in amyotrophic lateral sclerosis (ALS) motor neuron disease. To confirm the contribution of ANXA11 mutations to ALS, a large exome data set obtained from 330 French patients, including 150… read more here.
Keywords: genetic screening; anxa11 revealed; amyotrophic lateral; screening anxa11 ... See more keywords