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Identification of de novo mutations in the Chinese ASD cohort via whole-exome sequencing unveils brain regions implicated in autism

2021-07-22

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Autism spectrum disorder (ASD) is a highly heritable neurodevelopmental disorder characterized by deficits in social interactions and repetitive behaviors. Although hundreds of ASD risk genes, implicated in synaptic formation and transcriptional regulation, have been identified through human genetic studies, the East Asian ASD cohorts is still under-represented in the genome-wide genetic studies. Here we performed...

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Literature Corpus work: ba0257b8-3f6d-5373-9c2b-4c2d77c84623
DOI: 10.1101/2021.07.14.21260545

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Identification of de novo mutations in the Chinese ASD cohort via whole-exome sequencing unveils brain regions implicated in autismDOI 10.1101/2021.07.14.21260545Read

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Identification of <i>de novo</i> mutations in the Chinese ASD cohort via whole-exome sequencing unveils brain regions implicated in autism

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