Novel IRF6 mutations in Chinese Han families with Van der Woude syndrome

Novel IRF6 mutations in Chinese Han families with Van der Woude syndrome

Abstract Background Interferon Regulatory Factor 6 (IRF6) gene encodes a member of the IRF family of transcription factors. Mutations in IRF6 cause Van der Woude Syndrome (VWS), which is the most common malformation of syndromic orofacial clefts in humans. Methods Here, we performed sequencing studi...

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Bibliographic Details
Main Authors: Yanqin Yu, Yatao Wan, Chuanqi Qin, Haitang Yue, Zhuan Bian, Miao He
Format: Article
Language:English
Published: Wiley 2020-05-01
Series:Molecular Genetics & Genomic Medicine
Subjects:
Chinese Han
Interferon Regulatory Factor 6
sequencing study
Van der Woude syndrome
Online Access:https://doi.org/10.1002/mgg3.1196

Internet

https://doi.org/10.1002/mgg3.1196

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