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Reciprocal co-regulation of EGR2 and MECP2 is disrupted in Rett syndrome and autism
Mutations in MECP2, encoding methyl-CpG-binding protein 2 (MeCP2), cause the neurodevelopmental disorder Rett syndrome (RTT). Although MECP2 mutations are rare in idiopathic autism, reduced MeCP2 levels are common in autism cortex. MeCP2 is critical for postnatal neuronal maturation and a modulator...
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| Hlavní autoři: | , , , , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Oxford University Press
2009
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2638799/ https://ncbi.nlm.nih.gov/pubmed/19000991 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddn380 |
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