Recurrent mutation N383S and rare variants in PRKCI are causal for orofacial clefting and other phenotypes
Authors: Kelsey Robinson; Sunil K. Singh; Rachel Walkup; Dorelle V. Fawwal; Wasiu Lanre Adeyemo; Terri H. Beaty; Azeez Butali; Carmen J. Buxó; David J. Cutler; Michael P. Epstein; Brooklynn Gasser; Lord JJ Gowans; Jacqueline T. Hecht; Lina Moreno Uribe; Jeffrey C. Murray; Daryl Scott; Gary M. Shaw; Mary Ann Thomas; Seth M. Weinberg; Harrison Brand; Mary L. Marazita; Robert Lipinski; Robert A. Cornell; Elizabeth J. Leslie
Collaborators: Baylor College of Medicine; Emory University; Johns Hopkins University School of Medicine; Massachusetts General Hospital; Stanford; University of Calgary; University of Iowa; University of Pittsburgh School of Medicine; University of Texas Health Science Center at Houston; University of Washington; University of Wisconsin - Madison