The prevalence of the prothrombin gene variant C20209T in African-Americans and Caucasians and lack of association with venous thromboembolism
Author:
Publisher
Elsevier BV
Subject
Hematology
Reference6 articles.
1. 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
2. Prevalence of 20210A allele of the prothrombin gene in venous thromboembolism patients;Leroyer;Thromb Haemost,1998
3. Detection of a novel point mutation of the prothrombin gene at position 20209;Warshawsky;Diagn Mol Pathol,2002
4. Prevalence of the prothrombin 20210 G-to-A variant in blacks: infants, patients with venous thrombosis, patients with myocardial infarction, and control subjects;Dilley;J Lab Clin Med,1998
5. The 20210A allele of prothrombin is not found among sickle cell disease patients from West Africa;Rahimy;Thromb Haemost,1998
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1. F2c.*C20209T mutation in patients with a history of thrombosis: A case report, retrospective 2 site‐results and review of the literature;International Journal of Laboratory Hematology;2024-07-08
2. Coagulation Characterization of Prothrombin 20209C > T Variant: About 27 New Cases;Thrombosis and Haemostasis;2020-09-15
3. A Rare Prothrombin Gene Mutation C20209T in a South African Patient with Pulmonary Embolism in Pregnancy: a Case Study and Systematic Review;Clinical Laboratory;2019
4. Structure-function studies of prothrombin Amrita, a dysfunctional prothrombin characterized by point mutation at Arg553 → Gln;International Journal of Biological Macromolecules;2018-04
5. Medico-Legal Aspects of Pulmonary Thromboembolism;Advances in Experimental Medicine and Biology;2016
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