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Integrative approach to interpret DYRK1A variants, leading to a frequent neurodevelopmental disorder

Jérémie Courraud, Eric Chater‐Diehl, Benjamin Durand, Marie Vincent, Maria del Mar Muñiz Moreno, I. Boujelbene, Nathalie Drouot, Loréline Genschik, Élise Schaefer, Mathilde Nizon, Bénédicte Gérard, Marc Abramowicz, Benjamin Cogné, Lucas Bronicki, Lydie Bürglen, Magalie Barth, Perrine Charles, Estelle Colin, Christine Coubes, Albert David, Bruno Delobel, Florence Démurger, Sandrine Passemard, Anne‐Sophie Denommé‐Pichon, Laurence Faivre, Claire Feger, Mélanie Fradin, Christine Francannet, David Geneviève, Alice Goldenberg, Anne-Marie Guerrot, Bertrand Isidor, Katrine M. Johannesen, Boris Keren, Maria Kibæk, Paul Kuentz, Michèle Mathieu-Dramard, Bénédicte Demeer, Julia Métreau, Rikke S. Møller, Sébastien Moutton, Laurent Pasquier, Kristina P. Sørensen, Laurence Perrin, Mathilde Renaud, Pascale Saugier-Véber, Marlène Rio, Joane Svane, Julien Thévenon, Frédéric Tran Mau‐Them, Cathrine Elisabeth Tronhjem, Antonio Vitobello, Valérie Layet, Stéphane Auvin, Khaoula Khachnaoui, Marie‐Christine Birling, Séverine Drunat, Allan Bayat, Christèle Dubourg, Salima El Chehadeh, Christina Fagerberg, Cyril Mignot, Michel Guipponi, Thierry Bienvenu, Yann Hérault, Julie Thompson, Marjolaine Willems, Jean-Louis Mandel, Rosanna Weksberg, Amélie Piton

2021Genetics in Medicine35 citationsDOIOpen Access PDF

Topics & Concepts

Neurodevelopmental disorderDYRK1AMedicineAutism spectrum disorderMEDLINEPsychologyGeneticsPsychiatryBiologyDown syndromeAutismBiochemistryDown syndrome and intellectual disability researchGenetics and Neurodevelopmental DisordersDisability Rights and Representation
Integrative approach to interpret DYRK1A variants, leading to a frequent neurodevelopmental disorder | Litcius