Dominant mutations in GRHL3 cause Van der Woude Syndrome and disrupt oral periderm development.
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Am J Hum Genet. 2014 Jan 2;94(1):23-32. doi: 10.1016/j.ajhg.2013.11.009. Epub 2013 Dec 19.
Am J Hum Genet. 2014.
PMID: 24360809
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