The G20210A prothrombin gene mutation: is there room for screening families?
Open Access
- 10 August 2004
- journal article
- Published by Elsevier BV in Journal of Thrombosis and Haemostasis
- Vol. 2 (8), 1487-1488
- https://doi.org/10.1111/j.1538-7836.2004.00858.x
Abstract
No abstract availableThis publication has 6 references indexed in Scilit:
- The risk of venous thromboembolism in family members with mutations in the genes of factor V or prothrombin or bothBritish Journal of Haematology, 2000
- G20210A Mutation in Prothrombin Gene and Risk of Myocardial Infarction, Stroke, and Venous Thrombosis in a Large Cohort of US MenCirculation, 1999
- The G20210A Mutation of the Prothrombin Gene in Patients with Previous First Episodes of Deep-Vein Thrombosis: Prevalence and Association with Factor V G1691A, Methylenetetrahydrofolate Reductase C677T and Plasma Prothrombin LevelsThrombosis Research, 1999
- Increased Risk for Venous Thrombosis in Carriers of the Prothrombin G→A^20210 Gene VariantAnnals of Internal Medicine, 1998
- 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 thrombosisBlood, 1996