Rett syndrome from bench to bedside: recent advances [version 1; referees: 2 approved]
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 a...
| Main Authors: | , , , |
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| Format: | Article |
| Language: | English |
| Published: |
F1000 Research Ltd
2018-03-01
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| Series: | F1000Research |
| Online Access: | https://f1000research.com/articles/7-398/v1 |