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...

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Bibliographic Details
Main Authors: A. L. Petrin, E. Zeng, M. A. Thomas, D. Moretti-Ferreira, M. L. Marazita, X. J. Xie, J. C. Murray, L. M. Moreno-Uribe
Format: Article
Language:English
Published: Frontiers Media S.A. 2023-02-01
Series:Frontiers in Dental Medicine
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fdmed.2023.1120948/full