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Rett Syndrome and MeCP2

Rett syndrome (RTT) is a severe and progressive neurological disorder, which mainly affects young females. Mutations of the methyl-CpG binding protein 2 (MECP2) gene are the most prevalent cause of classical RTT cases. MECP2 mutations or altered expression are also associated with a spectrum of neur...

詳細記述

保存先:
書誌詳細
出版年:Neuromolecular Med
主要な著者: Liyanage, Vichithra R. B., Rastegar, Mojgan
フォーマット: Artigo
言語:Inglês
出版事項: 2014
主題:
オンライン・アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC5798978/
https://ncbi.nlm.nih.gov/pubmed/24615633
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s12017-014-8295-9
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