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The distinct methylation landscape of maturing neurons and its role in Rett Syndrome Pathogenesis
Rett syndrome (RTT) is one of the most common causes of intellectual and developmental disabilities in girls, and is caused by mutations in the gene encoding methyl-CpG binding protein 2 (MECP2). Here we will review our current understanding of RTT, the landscape of pathogenic mutations and function...
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| Publicado no: | Curr Opin Neurobiol |
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| Main Authors: | , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2019
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6892602/ https://ncbi.nlm.nih.gov/pubmed/31542590 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.conb.2019.08.001 |
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