Article

Mutation screening and burden analysis of GLT8D1 in Chinese patients with ALS

2020-05-13

Abstract excerpt

<title>Abstract</title> <p>Objective Glycosyltransfersase 8 domain containing 1 ( GLT8D1 ) gene was identified to be an amyotrophic lateral sclerosis (ALS) causative gene via pedigree co-segregation and burden analysis. However, validations based on large cohort of ALS among different ethnic population are essential. We aimed to systematically screen all exons of GLT8D1 in a large cohort of Chinese ALS patients,...

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Literature Corpus work: fc51546d-2105-5e56-8692-7229d9d6fe39
DOI: 10.21203/rs.3.rs-26967/v1

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