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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Detaylı Bibliyografya
Asıl Yazarlar: Lioy, Daniel T., Garg, Saurabh K., Monaghan, Caitlin E., Raber, Jacob, Foust, Kevin D., Kaspar, Brian K., Hirrlinger, Petra G., Kirchhoff, Frank, Bissonnette, John M., Ballas, Nurit, Mandel, Gail
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: 2011
Konular:
Article
Online Erişim: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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