Haemophilia A: molecular insights
Copyright policy )Haemophilia A: molecular insights
AbstractHaemophilia A is the most common inherited bleeding disorder caused by defects in theClin Chem Lab Med 2007;45:450–61.
- University Federico II of Naples Italy
- University of Molise Italy
Genetic Linkage, Genetic Carrier Screening, haemophilia A, factor VIII, haemophilia A, modifier genes, molecular analysis, prothrombotic gene variants, Genetic Therapy, factor VIII; F8C gene mutations; haemophilia A; modifier genes; molecular analysis; prothrombotic gene variants, Hemophilia A, prothrombotic gene variants, Introns, F8C gene mutations, factor VIII, modifier genes, Prenatal Diagnosis, Chromosome Inversion, Mutation, Humans, molecular analysis
Genetic Linkage, Genetic Carrier Screening, haemophilia A, factor VIII, haemophilia A, modifier genes, molecular analysis, prothrombotic gene variants, Genetic Therapy, factor VIII; F8C gene mutations; haemophilia A; modifier genes; molecular analysis; prothrombotic gene variants, Hemophilia A, prothrombotic gene variants, Introns, F8C gene mutations, factor VIII, modifier genes, Prenatal Diagnosis, Chromosome Inversion, Mutation, Humans, molecular analysis
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