den Hoed, Joeryde Boer, ElkeVoisin, NorineDingemans, Alexander J.M.Guex, NicolasWiel, LaurensNellaker, ChristofferAmudhavalli, Shivarajan M.Banka, SiddharthBena, Frederique S.Ben-Zeev, BruriaBonagura, Vincent R.Bruel, Ange-LineBrunet, TheresaBrunner, Han G.Chew, Hui B.Chrast, JacquelineCimbalistienė, LoretaCoon, HilaryDélot, Emmanuèlle C.Démurger, FlorenceDenommé-Pichon, Anne-SophieDepienne, ChristelDonnai, DianDyment, David A.Elpeleg, OrlyFaivre, LaurenceGilissen, ChristianGranger, LeslieHaber, BenjaminHachiya, YasuoAbedi, Yasmin HamzaviHanebeck, JenniferHehir-Kwa, Jayne Y.Horist, BrookeItai, ToshiyukiJackson, AdamJewell, RosalynJones, Kelly L.Joss, ShelaghKashii, HirofumiKato, MitsuhiroKattentidt-Mouravieva, Anja A.Kok, FernandoKotzaeridou, UraniaKrishnamurthy, VidyaKučinskas, VaidutisKuechler, AlmaLavillaureix, AlinoëLiu, PengfeiManwaring, LindaMatsumoto, NaomichiMazel, BenoîtMcWalter, KirstyMeiner, VardiellaMikati, Mohamad A.Miyatake, SatokoMizuguchi, TakeshiMoey, Lip H.Mohammed, ShehlaMor-Shaked, HagarMountford, HayleyNewbury-Ecob, RuthOdent, SylvieOrec, LauraOsmond, MatthewPalculict, Timothy B.Parker, MichaelPetersen, Andrea K.Pfundt, RolphPreikšaitienė, EglėRadtke, KellyRanza, EmmanuelleRosenfeld, Jill A.Santiago-Sim, TeresaSchwager, CaitlinSinnema, MargjeSnijders Blok, LotSpillmann, Rebecca C.Stegmann, Alexander P.A.Thiffault, IsabelleTran, LinhVaknin-Dembinsky, AdiVedovato-dos-Santos, Juliana H.Schrier Vergano, Samantha A.Vilain, EricVitobello, AntonioWagner, MatiasWaheeb, AndrouWilling, MarciaZuccarelli, BrittonKini, UshaNewbury, Dianne F.Kleefstra, TjitskeReymond, AlexandreFisher, Simon E.Vissers, Lisenka E.L.M.2023-04-122023-04-122023-04-12202110.1016/j.ajhg.2021.01.007https://infoscience.epfl.ch/handle/20.500.14299/196934Mutation-specific pathophysiological mechanisms define different neurodevelopmental disorders associated with SATB1 dysfunctiontext::journal::journal article::research article