학술논문
De novo variants in CNOT9 cause a neurodevelopmental disorder with or without epilepsy
Document Type
Article
Author
von Wintzingerode, L.; Hentschel, J.; Abou Jamra, R.; Oppermann, H.; Ben-Zeev, B.; Cesario, C.; Chan, K.M.; Bekheirnia, M.R.; Depienne, C.; Elpeleg, O.; Iascone, M.; Kelley, W.V.; Thompson, M.L.; Nassogne, M.-C.; Niceta, M.; Tartaglia, M.; Pezzani, L.; Rahner, N.; Revencu, N.; Santiago-Sim, T.; Trivisano, M.; Sticht, H.
Source
In: Genetics in Medicine . (Genetics in Medicine, July 2023, 25(7))
Subject
Language
English
ISSN
15300366
10983600
10983600