Phenotype-Genotype Correlation in Wilson Disease in a Large Lebanese Family: Association of c.2299insC with Hepatic and of p. Ala1003Thr with Neurologic Phenotype

• Julnar Usta,

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

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• Antonios Wehbeh,

  Affiliation Faculty of Medicine, American University of Beirut Medical Center, Beirut, Lebanon

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• Khaled Rida,

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

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• Omar El-Rifai,

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

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• Theresa Alicia Estiphan,

  Affiliation Faculty of Medicine, American University of Beirut Medical Center, Beirut, Lebanon

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• Tamar Majarian,

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

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• Kassem Barada

  * E-mail: kb02@aub.edu.lb

  Affiliation Division of Gastroenterology, Department of Internal Medicine, American University of Beirut Medical Center, Faculty of Medicine, Beirut, Lebanon

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