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A Critical and Cell-Autonomous Role for MeCP2 in Synaptic Scaling Up
Rett syndrome (Rett) is the leading genetic cause of mental retardation in females. Most cases of Rett are caused by loss-of-function mutations in the gene coding for the transcriptional regulator methyl-CpG binding protein 2 (MeCP2), but despite much effort, it remains unclear how a loss of MeCP2 f...
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| Main Authors: | , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Society for Neuroscience
2012
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3483036/ https://ncbi.nlm.nih.gov/pubmed/23015442 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1523/JNEUROSCI.3077-12.2012 |
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