Mutation-specific pathophysiological mechanisms in a new SATB1 -associated neurodevelopmental disorder
J. den Hoed, S. E. Fisher, B. Mazel(CHU Dijon Bourgogne), Alexandre Reymond(University of Lausanne), A. P. A. Stegmann(Maastricht University), Kelly L. Jones, Isabelle Thiffault(Children's Mercy Hospital), Margje Sinnema(Maastricht University Medical Centre), V. R. Bonagura, A.A. Kattentidt-Mouravieva, F. Demurger(Centre Hospitalier de Bretagne Sud), V. Krishnamurthy, C. Gilissen, Kelly Radtke(Ambry Genetics (United States)), Brooke Horist, A. Waheeb, C. Schwager, Lisenka E.L.M. Vissers(Radboud University Nijmegen), L. Faivre(CHU Dijon Bourgogne), C. Depienne, Shivarajan Amudhavalli(Children's Mercy Hospital), Linda Manwaring(Washington University in St. Louis), Britton Zuccarelli(University of Kansas), Jill A. Rosenfeld(Baylor College of Medicine), H. Brunner(Radboud University Nijmegen), Norine Voisin(University of Lausanne), Nicolas Guex(University of Lausanne), Dianne F. Newbury, Sara Mohammed, Antonio Vitobello(Inserm), E. Preiksaitiene, L. Granger, U. Kini, Yasmin Hamzavi Abedi, Elke de Boer(Radboud University Nijmegen), Ruth Newbury‐Ecob(University Hospitals Bristol NHS Foundation Trust), Lot Snijders Blok(Radboud University Nijmegen), K. Mcwalter, Emmanuelle Ranza(University Hospital of Geneva), A. Petersen, Tjitske Kleefstra(Radboud University Nijmegen), Jacqueline Chrast, S. Odent(CIC Rennes), Marcia Willing(Washington University in St. Louis), M. Osmond, A. Kuechler, Alinoë Lavillaureix(Centre National de la Recherche Scientifique)
HAL (Le Centre pour la Communication Scientifique Directe)
January 1, 2020
Cited by 1
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