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A novel pathogenic CDH3 variant underlying heredity hypotrichosis simplex detected by whole-exome sequencing (WES)-a case report

  • Ayat Kadhi
  • , Lamiaa Hamie
  • , Christel Tamer
  • , Georges Nemer*
  • , Mazen Kurban*
    • *Corresponding author for this work
  • Hamad bin Khalifa University
  • Sidra Medicine
  • American University of Beirut

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

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Biochemistry, Genetics and Molecular Biology