Mutation-specific pathophysiological mechanisms define different neurodevelopmental disorders associated with SATB1 dysfunction
Titel:
Mutation-specific pathophysiological mechanisms define different neurodevelopmental disorders associated with SATB1 dysfunction
Auteur:
den Hoed, Joery de Boer, Elke Voisin, Norine Dingemans, Alexander J.M. Guex, Nicolas Wiel, Laurens Nellaker, Christoffer Amudhavalli, Shivarajan M. Banka, Siddharth Bena, Frederique S. Ben-Zeev, Bruria Bonagura, Vincent R. Bruel, Ange-Line Brunet, Theresa Brunner, Han G. Chew, Hui B. Chrast, Jacqueline Cimbalistienė, Loreta Coon, Hilary Délot, Emmanuèlle C. Démurger, Florence Denommé-Pichon, Anne-Sophie Depienne, Christel Donnai, Dian Dyment, David A. Elpeleg, Orly Faivre, Laurence Gilissen, Christian Granger, Leslie Haber, Benjamin Hachiya, Yasuo Abedi, Yasmin Hamzavi Hanebeck, Jennifer Hehir-Kwa, Jayne Y. Horist, Brooke Itai, Toshiyuki Jackson, Adam Jewell, Rosalyn Jones, Kelly L. Joss, Shelagh Kashii, Hirofumi Kato, Mitsuhiro Kattentidt-Mouravieva, Anja A. Kok, Fernando Kotzaeridou, Urania Krishnamurthy, Vidya Kučinskas, Vaidutis Kuechler, Alma Lavillaureix, Alinoë Liu, Pengfei Manwaring, Linda Matsumoto, Naomichi Mazel, Benoît McWalter, Kirsty Meiner, Vardiella Mikati, Mohamad A. Miyatake, Satoko Mizuguchi, Takeshi Moey, Lip H. Mohammed, Shehla Mor-Shaked, Hagar Mountford, Hayley Newbury-Ecob, Ruth Odent, Sylvie Orec, Laura Osmond, Matthew Palculict, Timothy B. Parker, Michael Petersen, Andrea K. Pfundt, Rolph Preikšaitienė, Eglė Radtke, Kelly Ranza, Emmanuelle Rosenfeld, Jill A. Santiago-Sim, Teresa Schwager, Caitlin Sinnema, Margje Snijders Blok, Lot Spillmann, Rebecca C. Stegmann, Alexander P.A. Thiffault, Isabelle Tran, Linh Vaknin-Dembinsky, Adi Vedovato-dos-Santos, Juliana H. Schrier Vergano, Samantha A. Vilain, Eric Vitobello, Antonio Wagner, Matias Waheeb, Androu Willing, Marcia Zuccarelli, Britton Kini, Usha Newbury, Dianne F. Kleefstra, Tjitske Reymond, Alexandre Fisher, Simon E. Vissers, Lisenka E.L.M.