prothrombin G20210A mutation
Selected indexed studies
- Prothrombin G20210A Gene Mutation-Induced Recurrent Deep Vein Thrombosis and Pulmonary Embolism: Case Report and Literature Review. (J Investig Med High Impact Case Rep, 2022) [PMID:35426321]
- Prothrombin G20210A mutation and lower extremity peripheral arterial disease: a systematic review and meta-analysis. (Eur J Vasc Endovasc Surg, 2015) [PMID:26092622]
- Prothrombin G20210A mutation is associated with recurrent pregnancy loss: a systematic review and meta-analysis update. (Thromb Res, 2015) [PMID:25528068]
_Worker-drafted node — pending editorial review._
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Sources
- Prothrombin G20210A Gene Mutation-Induced Recurrent Deep Vein Thrombosis and Pulmonary Embolism: Case Report and Literature Review. (2022) pubmed
- Prothrombin G20210A mutation and lower extremity peripheral arterial disease: a systematic review and meta-analysis. (2015) pubmed
- Prothrombin G20210A mutation is associated with recurrent pregnancy loss: a systematic review and meta-analysis update. (2015) pubmed
- Prothrombin G20210A mutation is not associated with recurrent miscarriages. (2002) pubmed
- Prothrombin G20210A mutation, antithrombin, heparin cofactor II, protein C, and protein S defects. (2003) pubmed
- Prothrombin G20210A gene mutation, heparin cofactor II defects, primary (essential) thrombocythemia, and thrombohemorrhagic manifestations. (1999) pubmed
- The Association of Prothrombin Gene G20210A Mutation with Recurrent Venous Thromboembolism: Evidence from a Meta-Analysis. (2025) pubmed
- Clinical and laboratory management of the prothrombin G20210A mutation. (2002) pubmed
- Global prevalence of prothrombin gene mutation G20210A and implications in women's health: a systematic review. (2016) pubmed
- Prevalence of prothrombin G20210A mutation in patients with atrial fibrillation: A systematic review and meta-analysis. (2016) pubmed