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Mecp2 deficiency leads to delayed maturation and altered gene expression in hippocampal neurons
It is well known that Rett Syndrome, a severe postnatal childhood neurological disorder is mostly caused by mutations in the MECP2 gene. However, how deficiencies in MeCP2 contribute to the neurological dysfunction of Rett Syndrome is not clear. We aimed to resolve the role of MeCP2 epigenetic regul...
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| Main Authors: | , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2007
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2789309/ https://ncbi.nlm.nih.gov/pubmed/17532643 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.nbd.2007.04.005 |
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