De novo variants in CNOT9 cause a neurodevelopmental disorder with or without epilepsy
- Resource Type
- Article
- Authors
- von Wintzingerode, Lydia; Ben-Zeev, Bruria; Cesario, Claudia; Chan, Katie M.; Depienne, Christel; Elpeleg, Orly; Iascone, Maria; Kelley, Whitley V.; Nassogne, Marie-Cécile; Niceta, Marcello; Pezzani, Lidia; Rahner, Nils; Revencu, Nicole; Bekheirnia, Mir Reza; Santiago-Sim, Teresa; Tartaglia, Marco; Thompson, Michelle L.; Trivisano, Marina; Hentschel, Julia; Sticht, Heinrich; Abou Jamra, Rami; Oppermann, Henry
- Source
- In Genetics in Medicine July 2023 25(7)
- Subject
- Language
- ISSN
- 1098-3600