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:
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