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Rett syndrome from bench to bedside: recent advances
Rett Syndrome is a severe neurological disorder mainly due to de novo mutations in the methyl-CpG-binding protein 2 gene ( MECP2). Mecp2 is known to play a role in chromatin organization and transcriptional regulation. In this review, we report the latest advances on the molecular function of Mecp2...
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| Veröffentlicht in: | F1000Res |
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| Hauptverfasser: | , , , |
| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
F1000 Research Limited
2018
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| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5871944/ https://ncbi.nlm.nih.gov/pubmed/29636907 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.12688/f1000research.14056.1 |
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