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Apoptotic Activity of MeCP2 Is Enhanced by C-Terminal Truncating Mutations
Methyl-CpG binding protein 2 (MeCP2) is a widely abundant, multifunctional protein most highly expressed in post-mitotic neurons. Mutations causing Rett syndrome and related neurodevelopmental disorders have been identified along the entire MECP2 locus, but symptoms vary depending on mutation type a...
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| Publicado no: | PLoS One |
|---|---|
| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Public Library of Science
2016
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4956225/ https://ncbi.nlm.nih.gov/pubmed/27442528 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0159632 |
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