The risk of venous thromboembolism in family members with mutations in the genes of factor V or prothrombin or both
Author:
Publisher
Wiley
Subject
Hematology
Reference30 articles.
1. Increased risk of venous thrombosis in carriers of hereditary protein C deficiency defect
2. Prevalence of the Prothrombin Gene Variant (nt20210A) in Venous Thrombosis and Arterial Disease
3. Risk of venous thromboembolism associated with a G to A transition at position 20210 in the 3′-untranslated region of the prothrombin gene
4. Risk of Venous Thromboembolism and Clinical Manifestations in Carriers of Antithrombin, Protein C, Protein S Deficiency, or Activated Protein C Resistance
5. The G20210A Mutation of the Prothrombin Gene in Patients with Previous First Episodes of Deep-Vein Thrombosis
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