IRF6 and SPRY4 Signaling Interact in Periderm Development
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DOI: 10.1177/0022034517719870
Abstract: Rare mutations in IRF6 and GRHL3 cause Van der Woude syndrome, an autosomal dominant orofacial clefting disorder. Common variants in IRF6 and GRHL3 also contribute risk for isolated orofacial clefting. Similarly, variants within genes that… read more here.
Keywords: irf6 spry4; signaling interact; abnormal oral; irf6 ... See more keywords