Editorial: Epigenetic Mechanisms and Their Involvement in Rare Diseases

被引：10
|
作者：
Rastegar, Mojgan [1 ]
Yasui, Dag H. [2 ]
机构：
[1] Univ Manitoba, Rady Fac Hlth Sci, Dept Biochem & Med Genet, Max Rady Coll Med, Winnipeg, MB, Canada
[2] Univ Calif Davis, Sch Med, Dept Med Microbiol & Immunol, Davis, CA 95616 USA
来源：
FRONTIERS IN GENETICS | 2021年 / 12卷
基金：
加拿大自然科学与工程研究理事会; 美国国家卫生研究院;
关键词：
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;
D O I：
10.3389/fgene.2021.755076
中图分类号：
Q3 [遗传学];
学科分类号：
071007 ; 090102 ;
摘要：
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引用
收藏
页数：3
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