Single-Cell Transcriptomics Supports a Role of <i>CHD8</i> in Autism
Chromodomain helicase domain 8 (<i>CHD8</i>) is one of the most frequently mutated and most penetrant genes in the autism spectrum disorder (ASD). Individuals with <i>CHD8</i> mutations show leading symptoms of autism, macrocephaly, and facial dysmorphisms. The molecular and...
| Main Authors: | , |
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| Format: | Article |
| Language: | English |
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MDPI AG
2021-03-01
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| Series: | International Journal of Molecular Sciences |
| Subjects: | |
| Online Access: | https://www.mdpi.com/1422-0067/22/6/3261 |