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De novo variants in FBXO11 cause a syndromic form of intellectual disability with behavioral problems and dysmorphisms

  • Sandra Jansen
  • , Ilse M. van der Werf
  • , A. Micheil Innes
  • , Alexandra Afenjar
  • , Pankaj B. Agrawal
  • , Ilse J. Anderson
  • , Paldeep S. Atwal
  • , Ellen van Binsbergen
  • , Marie-Jose van den Boogaard
  • , Lucia Castiglia
  • , Zeynep H. Coban-Akdemir
  • , Anke van Dijck
  • , Diane Doummar
  • , Albertien M. van Eerde
  • , Anthonie J. van Essen
  • , Koen L. van Gassen
  • , Maria J. Guillen Sacoto
  • , Mieke M. van Haelst
  • , Ivan Iossifov
  • , Jessica L. Jackson
    • Elizabeth Judd, Charu Kaiwar, Boris Keren, Eric W. Klee, Jolien S. Klein Wassink-Ruiter, Marije E. Meuwissen, Kristin G. Monaghan, Sonja A. de Munnik, Caroline Nava, Charlotte W. Ockeloen, Rosa Pettinato, Hilary Racher, Tuula Rinne, Corrado Romano, Victoria R. Sanders, Rhonda E. Schnur, Eric J. Smeets, Alexander P. A. Stegmann, Asbjorg Stray-Pedersen, David A. Sweetser, Paulien A. Terhal, Kristian Tveten, Grace E. VanNoy, Petra F. de Vries, Jessica L. Waxler, Marcia Willing, Rolph Pfundt, Joris A. Veltman, R. Frank Kooy, Lisenka E. L. M. Vissers, Bert B. A. de Vries*
*Corresponding author for this work

Research output: Contribution to journal › Article › Academic › peer-review

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Biochemistry, Genetics and Molecular Biology