Biallelic null variants in ZNF142 cause global developmental delay with familial epilepsy and dysmorphic features

Added 34 days ago (17.09.2021)
Authors: Shinichi Kameyama; Takeshi Mizuguchi; Hiromi Fukuda; Lip Hen Moey; Wee Teik Keng; Nobuhiko Okamoto; Naomi Tsuchida; Yuri Uchiyama; Eriko Koshimizu; Kohei Hamanaka; Atsushi Fujita; Satoko Miyatake; Naomichi Matsumoto
Read article