@article{UBHD-68762899,
  author={Hoed, Joery den and de Boer, Elke and Voisin, Norine and Dingemans, Alexander J. M. and Guex, Nicolas and Wiel, Laurens and Nellaker, Christoffer and Amudhavalli, Shivarajan M. and Banka, Siddharth and Bena, Frederique S. and Ben-Zeev, Bruria and Bonagura, Vincent R. and Bruel, Ange-Line and Brunet, Theresa and Brunner, Han G. and Chew, Hui B. and Chrast, Jacqueline and Cimbalistienė, Loreta and Coon, Hilary and Délot, Emmanuèlle C. and Démurger, Florence and Denommé-Pichon, Anne-Sophie and Depienne, Christel and Donnai, Dian and Dyment, David A. and Elpeleg, Orly and Faivre, Laurence and Gilissen, Christian and Granger, Leslie and Haber, Benjamin and Hachiya, Yasuo and Abedi, Yasmin Hamzavi and Hanebeck, Jennifer and Hehir-Kwa, Jayne Y. and Horist, Brooke and Itai, Toshiyuki and Kotzaeridou, Urania and Orec, Laura},
  title={Mutation-specific pathophysiological mechanisms define different neurodevelopmental disorders associated with SATB1 dysfunction},
  year={2021},
  pages={346-356},
  language={eng},
  issn={1537-6605},
  volume={108},
  number={2 vom: Feb.},
  note={Gesehen am 24.07.2021},
  journal={The American journal of human genetics},
  doi={10.1016/j.ajhg.2021.01.007},
}