@misc{indiciae0b67fde94db7,
  title = {Mutation-specific pathophysiological mechanisms define different neurodevelopmental disorders associated with SATB1 dysfunction},
  author = {den Hoed, J. and Boer, E. d. and Voisin, N. and Dingemans, A. and Guex, N. and Wiel, L. and Nellaker, C. and Amudhavalli, S. and Banka, S. and Bena, F. and Ben-Zeev, B. and Bonagura, V. and Bruel, A.-L. and Brunet, T. and Brunner, H. and Chew, H. and Chrast, J. and Cimbalistien, L. and Coon, H. and Study, T. D. and Delot, E. and Demurger, F. and Denomme-Pichon, A.-S. and Depienne, C. and Donnai, D. and Dyment, D. and Elpeleg, O. and Faivre, L. and Gilissen, C. and Granger, L. and Haber, B. and Hachiya, Y. and Hamzavi Abedi, Y. and Hanebeck, J. and Hehir-Kwa, J. and Horist, B. and Itai, T. and Jackson, A. and Jewell, R. and Jones, K. and Joss, S. and Kashii, H. and Kato, M. and Kattentidt-Mouravieva, A. and Kok, F. and Kotzaer},
  year = {2020},
  doi = {10.1101/2020.10.23.352278},
  url = {https://www.biorxiv.org/content/10.1101/2020.10.23.352278v1},
  note = {Source identifier: 10.1101/2020.10.23.352278}
}