DNA methylation differences in monozygotic twins with Van der Woude syndrome
IntroductionVan der Woude Syndrome (VWS) is an autosomal dominant disorder responsible for 2% of all syndromic orofacial clefts (OFCs) with IRF6 being the primary causal gene (70%). Cases may present with lip pits and either cleft lip, cleft lip with cleft palate, or cleft palate, with marked phenot...
Main Authors: | , , , , , , , |
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Format: | Article |
Language: | English |
Published: |
Frontiers Media S.A.
2023-02-01
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Series: | Frontiers in Dental Medicine |
Subjects: | |
Online Access: | https://www.frontiersin.org/articles/10.3389/fdmed.2023.1120948/full |