An Association Between the Common Hereditary Hemochromatosis Mutation and the Factor V Leiden Allele in a Population With Thrombosis

This publication has 12 references indexed in Scilit:

• Thrombosis and Secondary Hemochromatosis Play Major Roles in the Pathogenesis of Jaundiced and Spherocytic Mice, Murine Models for Hereditary Spherocytosis
  Blood, 1997
• A Common Prothrombin Variant (20210 G to A) Increases the Risk of Myocardial Infarction in Young Women
  Blood, 1997
• Factor V Leiden (Resistance to Activated Protein C) Increases the Risk of Myocardial Infarction in Young Women
  Blood, 1997
• A common genetic variation in the 3'-untranslated region of the prothrombin gene is associated with elevated plasma prothrombin levels and an increase in venous thrombosis
  Blood, 1996
• Haemochromatosis and HLA–H
  Nature Genetics, 1996
• A novel MHC class I–like gene is mutated in patients with hereditary haemochromatosis
  Nature Genetics, 1996
• Genetic Hemochromatosis: Pathogenesis, Diagnosis, and Therapy
  Digestive Diseases, 1996
• Inherited thrombophilia: resistance to activated protein C as a pathogenic factor of venous thromboembolism
  Blood, 1995