DNMT3A Haploinsufficiency Results in Behavioral Deficits and Global Epigenomic Dysregulation Shared across Neurodevelopmental Disorders

Mutations in DNA methyltransferase 3A (DNMT3A) have been detected in autism and related disorders, but how these mutations disrupt nervous system function is unknown. Here, we define the effects of DNMT3A mutations associated with neurodevelopmental disease. We show that diverse mutations affect dif...

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Detalhes bibliográficos
Publicado no:Cell Rep
Main Authors: Christian, Diana L., Wu, Dennis Y., Martin, Jenna R., Moore, J. Russell, Liu, Yiran R., Clemens, Adam W., Nettles, Sabin A., Kirkland, Nicole M., Papouin, Thomas, Hill, Cheryl A., Wozniak, David F., Dougherty, Joseph D., Gabel, Harrison W.
Formato: Artigo
Idioma:Inglês
Publicado em: 2020
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7716597/
https://ncbi.nlm.nih.gov/pubmed/33238114
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.celrep.2020.108416
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