De novo variants in KDM2A cause a syndromic neurodevelopmental disorder

  • Eric N. Anderson
  • , Stephan Drukewitz
  • , Sukhleen Kour
  • , Anuradha V. Chimata
  • , Deepa S. Rajan
  • , Senta Schönnagel
  • , Karen L. Stals
  • , Deirdre Donnelly
  • , Siobhan O'Sullivan
  • , John F. Mantovani
  • , Tiong Y. Tan
  • , Zornitza Stark
  • , Pia Zacher
  • , Nicolas Chatron
  • , Pauline Monin
  • , Severine Drunat
  • , Yoann Vial
  • , Xenia Latypova
  • , Jonathan Levy
  • , Alain Verloes
    • Jennefer N. Carter, Devon E. Bonner, Suma P. Shankar, Jonathan A. Bernstein, Julie S. Cohen, Anne Comi, Deanna Alexis Carere, Lisa M. Dyer, Sureni V. Mullegama, Pedro A. Sanchez-Lara, Katheryn Grand, Hyung Goo Kim, Afif Ben-Mahmoud, Sidney M. Gospe, Rebecca S. Belles, Gary Bellus, Klaske D. Lichtenbelt, Renske Oegema, Anita Rauch, Ivan Ivanovski, Frederic Tran Mau-Them, Aurore Garde, Rachel Rabin, John Pappas, Annette E. Bley, Janna Bredow, Timo Wagner, Eva Decker, Carsten Bergmann, Louis Domenach, Henri Margot, Johannes R. Lemke, Rami Abou Jamra, Julia Hentschel, Heather Mefford, Amit Singh, Udai Bhan Pandey*, Konrad Platzer*
*Corresponding author for this work

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

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Biochemistry, Genetics and Molecular Biology