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Regulation of RNA splicing by the methylation-dependent transcriptional repressor methyl-CpG binding protein 2
Rett syndrome (RTT) is a postnatal neurodevelopmental disorder characterized by the loss of acquired motor and language skills, autistic features, and unusual stereotyped movements. RTT is caused by mutations in the X-linked gene encoding methyl-CpG binding protein 2 (MeCP2). Mutations in MECP2 caus...
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| Main Authors: | , , , , , , , , , , |
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| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
National Academy of Sciences
2005
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| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1266160/ https://ncbi.nlm.nih.gov/pubmed/16251272 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.0507856102 |
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