Human KCNQ5 de novo mutations underlie epilepsy and intellectual disability
人类KCNQ5基因的新生突变是癫痫和智力障碍的根本原因。
期刊:Journal of Neurophysiology
影响因子:2.1
doi:10.1152/jn.00509.2021
Wei, Aguan D; Wakenight, Paul; Zwingman, Theresa A; Bard, Angela M; Sahai, Nikhil; Willemsen, Marjolein H; Schelhaas, Helenius J; Stegmann, Alexander P A; Verhoeven, Judith S; de Man, Stella A; Wessels, Marja W; Kleefstra, Tjitske; Shinde, Deepali N; Helbig, Katherine L; Basinger, Alice; Wagner, Victoria F; Rodriguez-Buritica, David; Bryant, Emily; Millichap, John J; Millen, Kathleen J; Dobyns, William B; Ramirez, Jan-Marino; Kalume, Franck K