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Functional consequences of Rett syndrome mutations on human MeCP2

The neurodevelopmental disorder known as Rett syndrome has recently been linked to the methyl-CpG-binding transcriptional repressor, MeCP2. In this report we examine the consequences of these mutations on the function of MeCP2. The ability to bind specifically to methylated DNA and the transcription...

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Bibliografiske detaljer
Main Authors: Yusufzai, Timur M., Wolffe, Alan P.
Format: Artigo
Sprog:Inglês
Udgivet: Oxford University Press 2000
Fag:
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC113135/
https://ncbi.nlm.nih.gov/pubmed/11058114
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