Comprehensive Analysis of CNOT3-related Neurodevelopmental Disorders: Phenotypic and Genotypic Characterization.
Camille Engel, Michaela Rendek, Jessica Assoumani,Emanuela Argilli,Francesca Ariani, Anne-Laude Avice-Denizet, Emilia K Bijlsmaa, Pierre Blanc, Lucia Pia Bruno,Bert Callewaert,Valeria Capra, Michele Carullo,Bertrand Chesneau,Sandra Coppens,Cynthia Curry,Breanne Dale, Eric Dahlen, Andrée Delahaye-Duriez, Anne-Sophie Denommé-Pichon,Bénédicte Demeer, Lenka Dvořáková, Jan Fischer,David Geneviève,Thea Giacomini, Mette M Handrup,Delphine Heron, Irina Hüning, Michelle Iacomino,Bertrand Isidor,Boris Keren,Stanislav Kmoch,David A Koolen, Andrea Kübler, Jana Laštůvková, Carolyn Le,Jonathan Levy, Caterina Lo Rizzo,Silvia Maitz,Sandrine Marlin,Cyril Mignot, Ghayda Mirzaa,Inga Nagel, Sebastian Neuens,Lenka Nosková,Emily Pao, Anna Pecková,Julie Plaisancie,Joseph Porrmann,Flavia Privitera,André Reis,Alessandra Renieri,Marlène Rio, Alyssa Rippert,Lukáš Ryba, Marcello Scala, Jolanda H Schieving,Elliott H Sherr, Andrew Shuen,Richard Sidlow, Thomas Smol,Julie Soblet,Pasquale Striano,Mohnish Suri, Hannes Syryn, Frédéric Tran Mau-Them, Andre M Travessa, Julien Van Gils,Georgia Vasileiou, Jolijn J A Verseput,Catheline Vilain,Catherine Vincent-Delorme,Emílie Vyhnálková, Emma L Wakeling,Pia Zacher,Federico Zara,Paul Kuentz,Juliette Piard European journal of human genetics EJHG（2025）
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