Skip to main navigation Skip to search Skip to main content

A Novel Mutation in FOXC1 in a Lebanese Family with Congenital Heart Disease and Anterior Segment Dysgenesis: Potential Roles for NFATC1 and DPT in the Phenotypic Variations

  • Athar Khalil
  • , Christiane Al-Haddad
  • , Hadla Hariri
  • , Kamel Shibbani
  • , Fadi Bitar
  • , Mazen Kurban
  • , Georges Nemer*
  • , Mariam Arabi
    • *Corresponding author for this work
  • American University of Beirut
  • Columbia University

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

15   Link opens in a new tab Citations (Scopus)

Fingerprint

Dive into the research topics of 'A Novel Mutation in FOXC1 in a Lebanese Family with Congenital Heart Disease and Anterior Segment Dysgenesis: Potential Roles for NFATC1 and DPT in the Phenotypic Variations'. Together they form a unique fingerprint.
Sort by

Biochemistry, Genetics and Molecular Biology

Immunology and Microbiology

Keyphrases

Medicine and Dentistry