Molecular Phenotype of Constitutional TET2 Haploinsufficiency in Humans
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资源简介：
In this study, we observed the effects of constitutional heterozygous TET2 loss on blood DNA methylation, chromatin activity and gene expression in carriers of truncating TET2 germline mutations. To provide additional context to findings in TET2 mutation carriers, we analysed DNA methylation in four DNMT3A germline mutation carriers and their age-matched controls.EGA study EGAS00001003454
创建时间：
2019-03-05
