Single-Cell Transcriptomics Supports a Role of CHD8 in Autism
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DOI: 10.3390/ijms22063261
Abstract: Chromodomain helicase domain 8 (CHD8) is one of the most frequently mutated and most penetrant genes in the autism spectrum disorder (ASD). Individuals with CHD8 mutations show leading symptoms of autism, macrocephaly, and facial dysmorphisms.… read more here.
Keywords: single cell; transcriptomics supports; autism; cell transcriptomics ... See more keywords