Article
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 - 1 Oct 2024
Jambou Didier, Saut Noemie, Queyrel Viviane, Appert-Flory Anny, Fischer Florence, Suchon Pierre, De Pooter Neila, Toulon Pierre
Abstract excerpt
INTRODUCTION: G20210A (c.*97G>A) prothrombin gene variant, found in white population has been associated with an increased risk of venous thromboembolism (VTE). Other rare polymorphisms in F2 gene (C20209T) have been reported, more rare and touching black people, but its potential association with VTE remain uncertain. METHODS: About a 69 years-old Caucasian woman presenting an unprovoked deep venous thrombosis...
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