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Single-Cell Transcriptomics Supports a Role of CHD8 in Autism
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. The molecular and cellular mechanisms underpinning the e...
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| Veröffentlicht in: | Int J Mol Sci |
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| Hauptverfasser: | , |
| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
MDPI
2021
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| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8004931/ https://ncbi.nlm.nih.gov/pubmed/33806835 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/ijms22063261 |
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