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A role for glia in the progression of Rett syndrome
Rett syndrome (RTT) is an X-chromosome-linked autism spectrum disorder caused by loss of function of the transcription factor methyl CpG-binding protein 2 (MeCP2)(1). Although MeCP2 is expressed in most tissues(2), loss of MeCP2 results primarily in neurological symptoms(1,3,4). Earlier studies prop...
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| Главные авторы: | , , , , , , , , , , |
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| Формат: | Artigo |
| Язык: | Inglês |
| Опубликовано: |
2011
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| Предметы: | |
| Online-ссылка: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3268776/ https://ncbi.nlm.nih.gov/pubmed/21716289 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/nature10214 |
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