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MeCP2: The Genetic Driver of Rett Syndrome Epigenetics
Mutations in methyl CpG binding protein 2 (MeCP2) are the major cause of Rett syndrome (RTT), a rare neurodevelopmental disorder with a notable period of developmental regression following apparently normal initial development. Such MeCP2 alterations often result in changes to DNA binding and chroma...
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| Publicat a: | Front Genet |
|---|---|
| Autors principals: | , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Frontiers Media S.A.
2021
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7859524/ https://ncbi.nlm.nih.gov/pubmed/33552148 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fgene.2021.620859 |
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