De novo variants in CELF2 that disrupt the nuclear localization signal cause developmental and epileptic encephalopathy - Itai, Toshiyuki; Hamanaka, Kohei; Sasaki, Kazunori; Wagner, Matias; Kotzaeridou, Urania; Brösse, Ines; Ries, Markus; Kobayashi, Yu; Tohyama, Jun; Kato, Mitsuhiro; Ong, Winnie P.; Chew, Hui B.; et al. (Human mutation, 2021)
First published: 01 November 2020