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Novel Digital Anomalies, Hippocampal Atrophy, and Mutations Expand the Genotypic and Phenotypic Spectra of CNKSR2 in the Houge Type of X-Linked Syndromic Intellectual Development Disorder (MRXSHG)

  • Mohammad Reza Ghasemi
  • , Sahand Tehrani Fateh
  • , Afif Ben-Mahmoud
  • , Vijay Gupta
  • , Lara G. Stühn
  • , Gaetan Lesca
  • , Nicolas Chatron
  • , Konrad Platzer
  • , Patrick Edery
  • , Hossein Sadeghi
  • , Bertrand Isidor
  • , Benjamin Cogné
  • , Heidi L. Schulz
  • , Ilona Krauspe-Stübecke
  • , Radhakrishnan Periyasamy
  • , Sheela Nampoothiri
  • , Reza Mirfakhraie
  • , Sahar Alijanpour
  • , Steffen Syrbe
  • , Ulrich Pfeifer
    • Stephanie Spranger, Kathrin Grundmann-Hauser, Tobias B. Haack, Maria T. Papadopoulou, Tayrine da Silva Gonçalves, Eleni Panagiotakaki, Alexis Arzimanoglou, Seyed Hassan Tonekaboni, Massimiliano Rossi, G. Christoph Korenke, Yves Lacassie, Mi Hyeon Jang, Lawrence C. Layman, Mohammad Miryounesi, Hyung Goo Kim*
*Corresponding author for this work

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

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Biochemistry, Genetics and Molecular Biology