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Acute and crucial requirement for MeCP2 function upon transition from early to late adult stages of brain maturation
Germline mutations in the X-linked gene, methyl-CpG-binding protein 2 (MECP2), underlie most cases of Rett syndrome (RTT), an autism spectrum disorder affecting approximately one in 10 000 female live births. The disease is characterized in affected girls by a latent appearance of symptoms between 1...
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| Pubblicato in: | Hum Mol Genet |
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| Autori principali: | , , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Oxford University Press
2016
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4986326/ https://ncbi.nlm.nih.gov/pubmed/26908602 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddw038 |
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