An Association Between the Common Hereditary Hemochromatosis Mutation and the Factor V Leiden Allele in a Population With Thrombosis
Author:
Affiliation:
1. Department of Pathology
2. Queen’s University
3. Kingston, Ontario, Canada
Publisher
American Society of Hematology
Subject
Cell Biology,Hematology,Immunology,Biochemistry
Reference9 articles.
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2. 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.;Poort;Blood,1996
3. Factor V Leiden (resistance to activated protein C) increases the risk of myocardial infarction in young women.;Rosendaal;Blood,1997
4. A common prothrombin variant (20210 G to A) increases the risk of myocardial infarction in young women.;Rosendaal;Blood,1997
5. A novel MHC class I-like gene is mutated in patients with herediatry hemochromatosis.;Feder;Nat Genet,1996
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