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The enhancement of activity rescues the establishment of Mecp2 null neuronal phenotypes
MECP2 mutations cause Rett syndrome (RTT), a severe and progressive neurodevelopmental disorder mainly affecting females. Although RTT patients exhibit delayed onset of symptoms, several evidences demonstrate that MeCP2 deficiency alters early development of the brain. Indeed, during early maturatio...
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| Publicado no: | EMBO Mol Med |
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| Principais autores: | , , , , , , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
John Wiley and Sons Inc.
2021
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8033520/ https://ncbi.nlm.nih.gov/pubmed/33665914 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.15252/emmm.202012433 |
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