Two Heterozygous Mutations in NFATC1 in a Patient with Tricuspid Atresia

• Zahi Abdul-Sater,

  Affiliation Department of Biochemistry and Molecular Genetics, American University of Beirut, Beirut, Lebanon

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• Amin Yehya,

  Affiliation Department of Biochemistry and Molecular Genetics, American University of Beirut, Beirut, Lebanon

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• Jean Beresian,

  Affiliation Department of Biochemistry and Molecular Genetics, American University of Beirut, Beirut, Lebanon

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• Elie Salem,

  Affiliation Department of Biochemistry and Molecular Genetics, American University of Beirut, Beirut, Lebanon

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• Amina Kamar,

  Affiliation Department of Biochemistry and Molecular Genetics, American University of Beirut, Beirut, Lebanon

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• Serine Baydoun,

  Affiliation Department of Biochemistry and Molecular Genetics, American University of Beirut, Beirut, Lebanon

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• Kamel Shibbani,

  Affiliation Department of Biochemistry and Molecular Genetics, American University of Beirut, Beirut, Lebanon

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• Ayman Soubra,

  Affiliation Department of Biochemistry and Molecular Genetics, American University of Beirut, Beirut, Lebanon

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• Fadi Bitar ,

  * E-mail: fadi.bitar@aub.edu.lb (FB); gn08@aub.edu.lb (GN)

  Affiliation Department of Pediatrics and Adolescent Medicine, American University of Beirut, Beirut, Lebanon

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• Georges Nemer

  * E-mail: fadi.bitar@aub.edu.lb (FB); gn08@aub.edu.lb (GN)

  Affiliation Department of Biochemistry and Molecular Genetics, American University of Beirut, Beirut, Lebanon

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