Loss-of-Function Variants in CUL3 Cause a Syndromic Neurodevelopmental Disorder

Patrick R. Blackburn, Frédéric Ebstein, Tzung Chien Hsieh, Marialetizia Motta, Francesca Clementina Radio, Johanna C. Herkert, Tuula Rinne, Isabelle Thiffault, Michele Rapp, Mariel Alders, Saskia Maas, Bénédicte Gerard, Thomas Smol, Catherine Vincent-Delorme, Benjamin Cogné, Bertrand Isidor, Marie Vincent, Ruxandra Bachmann-Gagescu, Anita Rauch, Pascal JosetGiovanni Battista Ferrero, Andrea Ciolfi, Thomas Husson, Anne Marie Guerrot, Carlos Bacino, Colleen Macmurdo, Stephanie S. Thompson, Jill A. Rosenfeld, Laurence Faivre, Frederic Tran Mau-Them, Wallid Deb, Virginie Vignard, Pankaj B. Agrawal, Jill A. Madden, Alice Goldenberg, François Lecoquierre, Michael Zech, Holger Prokisch, Ján Necpál, Robert Jech, Juliane Winkelmann, Monika Turčanová Koprušáková, Vassiliki Konstantopoulou, John R. Younce, Marwan Shinawi, Chloe Mighton, Charlotte Fung, Chantal F. Morel, Jordan Lerner-Ellis, Stephanie DiTroia, Magalie Barth, Dominique Bonneau, Ingrid Krapels, Alexander P.A. Stegmann, Vyne van der Schoot, Theresa Brunet, Cornelia Bußmann, Cyril Mignot, Giuseppe Zampino, Saskia B. Wortmann, Johannes A. Mayr, René G. Feichtinger, Thomas Courtin, Claudia Ravelli, Boris Keren, Alban Ziegler, Linda Hasadsri, Pavel N. Pichurin, Eric W. Klee, Katheryn Grand, Pedro A. Sanchez-Lara, Elke Krüger, Stéphane Bézieau, Hannah Klinkhammer, Peter Michael Krawitz, Evan E. Eichler, Marco Tartaglia, Sébastien Küry, Tianyun Wang

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Biochemistry, Genetics and Molecular Biology