Prothrombin Gene Mutation (G20210A) is Not Associated with Nonvalvular Atrial Fibrillation with Ischemic Stroke in Turkish Population

PP-092 Prothrombin G20210A is a genetic variant that approximately doubles or triples the risk of forming blood clots in the veins. The polymorphism is located in a noncoding region of the prothrombin gene (3' untranslated region nucleotide 20210), replacing guanine (G) with adenine (A). The