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Rett syndrome: disruption of epigenetic control of postnatal neurological functions
Loss-of-function mutations in the X-linked gene Methyl-CpG-binding protein 2 (MECP2) cause a devastating pediatric neurological disorder called Rett syndrome. In males, these mutations typically result in severe neonatal encephalopathy and early lethality. On the other hand, owing to expression of t...
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| Veröffentlicht in: | Hum Mol Genet |
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| Hauptverfasser: | , |
| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
Oxford University Press
2015
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| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4571996/ https://ncbi.nlm.nih.gov/pubmed/26060191 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddv217 |
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