Editorial: Epigenetic Mechanisms And Their Involvement In Rare Diseases
FRONTIERS IN GENETICS（2021）
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epigenetics and rare diseases, MeCP2 isoforms and rett syndrome (RTT), DNA methylation and histone modifications, ATRX and gene regulatory mechanisms, activity dependent neuroprotective protein (ADNP) and chromatin remodeling, Beckwith-Wiedemann Syndrome (BWS) and Prader-Willi Syndrome (PWS), O-linked-D-N-acetylglucosamine (O-GlcNAc), MYCN-related epigenetic factors and non-coding regulatory RNAs
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