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Variable expressivity and co-occurrence of LDLR and LDLRAP1 mutations in familial hypercholesterolemia: failure of the dominant and recessive dichotomy.
Fahed, Akl C; Khalaf, Ruby; Salloum, Rony; Andary, Rabih R; Safa, Raya; El-Rassy, Inaam; Moubarak, Elie; Azar, Sami T; Bitar, Fadi F; Nemer, Georges.
Afiliação
  • Fahed AC; Department of Biochemistry and Molecular GeneticsAmerican University of BeirutBeirutLebanon; Department of GeneticsHarvard Medical School and Department of Internal MedicineMassachusetts General HospitalBostonMassachusetts.
  • Khalaf R; Department of Biochemistry and Molecular Genetics American University of Beirut Beirut Lebanon.
  • Salloum R; Department of Biochemistry and Molecular Genetics American University of Beirut Beirut Lebanon.
  • Andary RR; Department of Biochemistry and Molecular Genetics American University of Beirut Beirut Lebanon.
  • Safa R; Department of Biochemistry and Molecular Genetics American University of Beirut Beirut Lebanon.
  • El-Rassy I; Department of Biochemistry and Molecular Genetics American University of Beirut Beirut Lebanon.
  • Moubarak E; National LDL Apheresis Center Dahr El-Bashek Governmental University Hospital Roumieh Lebanon.
  • Azar ST; Department of Internal Medicine American University of Beirut Beirut Lebanon.
  • Bitar FF; Department of Pediatrics and Adolescent Medicine American University of Beirut Beirut Lebanon.
  • Nemer G; Department of Biochemistry and Molecular Genetics American University of Beirut Beirut Lebanon.
Mol Genet Genomic Med ; 4(3): 283-91, 2016 May.
Article em En | MEDLINE | ID: mdl-27247956
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Mol Genet Genomic Med Ano de publicação: 2016 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Mol Genet Genomic Med Ano de publicação: 2016 Tipo de documento: Article