<i>SETBP1</i> variants outside the degron disrupt DNA-binding and transcription independent of protein abundance to cause a heterogeneous neurodevelopmental disorder
Maggie M. K. Wong(Max Planck Institute for Psycholinguistics), Simon E. Fisher(Radboud University Nijmegen), Gökberk Alagöz(Max Planck Institute for Psycholinguistics), Sacha Weber(Centre Hospitalier Universitaire de Caen Normandie), Giovanni Battista Ferrero(5T Torino (Italy)), Alice Moroni(University of Turin), Arianna Vino(Max Planck Institute for Psycholinguistics), Ruth Braden(The University of Melbourne), Samantha J. Turner(The University of Melbourne), Wendy K. Chung(Oregon Health & Science University), Francesca Novara(University of Pavia), Meghan Barnett(Women's and Children's Hospital), Lucinda Murray(Hunter Genetics), Aglaia Vignoli(University of Milan), David Mowat(UNSW Sydney), Ingrid E. Scheffer(The University of Melbourne), Michael S. Hildebrand, Angela Peron(University of Milan), Christopher Barnett(Women's and Children's Hospital), Frances Elmslie(St George’s University Hospitals NHS Foundation Trust), Fabio Sirchia(IRCCS Materno Infantile Burlo Garofolo), Rosalie A. Kampen(Max Planck Institute for Psycholinguistics), Elizabeth E. Palmer(The University of Sydney), Alexander J.M. Dingemans(Radboud University Nijmegen), Alfredo Brusco(Azienda Ospedaliera Citta' della Salute e della Scienza di Torino), Angela Morgan(The University of Melbourne), Diana Carli(University of Turin), Nadieh A. Jansen(Radboud University Nijmegen), Ingrid M.B.H. van de Laar(Erasmus MC), Marion Gérard(Université de Caen Normandie), Bregje W.M. van Bon(Radboud University Nijmegen), Bert Ba de Vries(Radboud University Nijmegen), V. López-González(Instituto de Salud Carlos III)
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