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Loss of histone methyltransferase ASH1L in the developing mouse brain causes autistic-like behaviors
Autism spectrum disorder (ASD) is a neurodevelopmental disease associated with various gene mutations. Recent genetic and clinical studies report that mutations of the epigenetic gene ASH1L are highly associated with human ASD and intellectual disability (ID). However, the causality and underlying m...
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| Publicado no: | Commun Biol |
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| Main Authors: | , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Nature Publishing Group UK
2021
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8213741/ https://ncbi.nlm.nih.gov/pubmed/34145365 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s42003-021-02282-z |
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