Recurrent mutation N383S and rare variants in PRKCI are causal for orofacial clefting and other phenotypes

Date:
Tuesday, Sep 10, 2024 5:00pm – 8:00pm
Conference:
SCGDB 2024
Authors:
Azeez Butali, Brooklynn Gasser, Carmen J. Buxó, Daryl Scott, David J. Cutler, Dorelle V. Fawwal, Elizabeth J. Leslie, Gary M. Shaw, Harrison Brand, Jacqueline T. Hecht, Jeffrey C. Murray, Kelsey Robinson, Lina Moreno Uribe, Lord JJ Gowans, Mary Ann Thomas, Mary L. Marazita, Michael P. Epstein, Rachel Walkup, Robert A. Cornell, Robert Lipinski, Seth M. Weinberg, Sunil K. Singh, Terri H. Beaty, Wasiu Lanre Adeyemo