Article
8p21.3 deletions are rare causes of non-syndromic autism spectrum disorder.
Neurogenetics - 1 Jul 2021
Cosemans Nele, Maljaars Jarymke, Vogels Annick, Holvoet Maureen, Devriendt Koen, Steyaert Jean, Van Den Bogaert Kris, Noens Ilse, Peeters Hilde
Abstract excerpt
A de novo 0.95 Mb 8p21.3 deletion had been identified in an individual with non-syndromic autism spectrum disorder (ASD) through high-resolution copy number variant analysis. Subsequent screening of in-house and publicly available databases resulted in the identification of six additional individuals with 8p21.3 deletions. Through case-based reasoning, we conclude that 8p21.3 deletions are rare causes of...
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