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- W2785627720 abstract "Rett syndrome is a neurodevelopmental disorder that primarily affects females and is caused by mutations in the methyl-CpG-binding-protein 2 (MECP2) gene. Initially, MeCP2 had been shown to be a repressor of gene transcription. In their 2008 paper, Chahrour and colleagues (DOI: 10.1126/science.1153252) reported that MeCP2 could also function as a transcriptional activator." @default.
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- W2785627720 date "2018-02-01" @default.
- W2785627720 modified "2023-10-01" @default.
- W2785627720 title "MeCP2 as an Activator of Gene Expression" @default.
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- W2785627720 doi "https://doi.org/10.1016/j.tins.2017.11.005" @default.
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