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Etiological involvement of KCND1 variants in an X-linked neurodevelopmental disorder with variable expressivity

  • Tassja Kalm
  • , Claudia Schob
  • , Hanna Völler
  • , Thatjana Gardeitchik
  • , Christian Gilissen
  • , Rolph Pfundt
  • , Chiara Klöckner
  • , Konrad Platzer
  • , Annick Klabunde-Cherwon
  • , Markus Ries
  • , Steffen Syrbe
  • , Francesca Beccaria
  • , Francesca Madia
  • , Marcello Scala
  • , Federico Zara
  • , Floris Hofstede
  • , Marleen E H Simon
  • , Richard H van Jaarsveld
  • , Renske Oegema
  • , Koen L I van Gassen
    • Sjoerd J B Holwerda, Tahsin Stefan Barakat, Arjan Bouman, Marjon van Slegtenhorst, Sara Álvarez, Alberto Fernández-Jaén, Javier Porta, Andrea Accogli, Margherita Maria Mancardi, Pasquale Striano, Michele Iacomino, Jong-Hee Chae, SeSong Jang, Soo Y Kim, David Chitayat, Saadet Mercimek-Andrews, Christel Depienne, Antje Kampmeier, Alma Kuechler, Harald Surowy, Enrico Silvio Bertini, Francesca Clementina Radio, Cecilia Mancini, Simone Pizzi, Marco Tartaglia, Lucas Gauthier, David Genevieve, Mylène Tharreau, Noy Azoulay, Gal Zaks-Hoffer, Nesia K Gilad, Naama Orenstein, Geneviève Bernard, Isabelle Thiffault, Jonas Denecke, Theresia Herget, Fanny Kortüm, Christian Kubisch, Robert Bähring*, Stefan Kindler
*Corresponding author for this work

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

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Biochemistry, Genetics and Molecular Biology