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Novel IRF6 mutations in Chinese patients with Van der Woude syndrome.

Journal of dental research - 1 Oct 2006

Du X, Tang W, Tian W, Li S, Li X, Liu L, Zheng X, Chen X, Lin Y, Tang Y

Abstract excerpt

Van der Woude syndrome (VWS) (OMIM 119300) is a dominantly inherited, developmental disorder that is characterized by pits and/or sinuses of the lower lip and a cleft lip and/or cleft palate. Mutations in the interferon regulatory factor 6 gene (IRF6) have been recently identified in patients with VWS, with more than 60 mutations reported. However, the VWS phenotype, IRF6 mutation genotypes, and their...

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Asian People
Cleft Lip
Cleft Palate
Craniofacial Abnormalities
Genetic Linkage

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Interferon Regulatory Factors

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PMID: 16998136
DOI: 10.1177/154405910608501013

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