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Mouse models of MeCP2 disorders share gene expression changes in the cerebellum and hypothalamus
A group of post-natal neurodevelopmental disorders collectively referred to as MeCP2 disorders are caused by aberrations in the gene encoding methyl-CpG-binding protein 2 (MECP2). Loss of MeCP2 function causes Rett syndrome (RTT), whereas increased copy number of the gene causes MECP2 duplication or...
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| Autori principali: | , , , , |
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| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Oxford University Press
2009
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2694691/ https://ncbi.nlm.nih.gov/pubmed/19369296 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddp181 |
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