Dominant mutations in GRHL3 cause Van der Woude syndrome and disrupt oral periderm development

Myriam Peyrard-Janvid*, Elizabeth J. Leslie, Youssef A. Kousa, Tiffany L. Smith, Martine Dunnwald, Måns Magnusson, Brian A. Lentz, Per Unneberg, Ingegerd Fransson, Hannele K. Koillinen, Jorma Rautio, Marie Pegelow, Agneta Karsten, Lina Basel-Vanagaite, William Gordon, Bogi Andersen, Thomas Svensson, Jeffrey C. Murray, Robert A. Cornell, Juha KereBrian C. Schutte

*Corresponding author for this work

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Medicine & Life Sciences