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Unexpected cellular players in Rett syndrome pathology
Rett syndrome is a devastating neurodevelopmental disorder, primarily caused by mutations of methyl CpG-binding protein 2 (MeCP2). Although the genetic cause of disease was identified over a decade ago, a significant gap still remains in both our clinical and scientific understanding of its pathogen...
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| Publicado no: | Neurobiol Dis |
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| Principais autores: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2015
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4644494/ https://ncbi.nlm.nih.gov/pubmed/25982834 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.nbd.2015.05.005 |
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