DNA Methylation in the Diagnosis of Monogenic Diseases
Abstract
DNA methylation in the human genome is largely programmed and shaped by transcription factor binding and interaction between DNA methyltransferases and histone marks during gamete and embryo development. Normal methylation profiles can be modified at single or multiple loci, more frequently as consequences of genetic variants acting in cis or in trans, or in some cases stochastically or through interaction with environmental factors. For many...
Paper Details
Title
DNA Methylation in the Diagnosis of Monogenic Diseases
Published Date
Mar 26, 2020
Journal
Volume
11
Issue
4
Pages
355 - 355
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