Gül, Enes ElvinErdoğan, Halil İbrahimBayram, Ufuk TanÖzdemir, KurtuluşTaşçı, İlker2020-03-262020-03-262012Gül, E. E., Erdoğan, H. İ., Bayram, U. T., Özdemir, K., Taşçı, İ., (2012). Mobile Right Heart Thrombus as a Manifestation of Homozygous Mutation of Mthfr 1298 a>c. Anatolian Journal of Cardiology, 12(6), 527-528. Doi:10.5152/akd.2012.1672149-22632149-2271https://dx.doi.org/10.5152/akd.2012.168https://hdl.handle.net/20.500.12395/28236Mobile right heart thrombus (MRHT) is uncommon pathology but the true prevalence is still unknown. Previous studies reported that MRHT occurs in 7% to 18% of patients with pulmonary embolism with high mortality rate (44.7%) (1). The main manifestations of venous thromboembolism (VTE) are deep venous thrombosis (DVT) and pulmonary embolism. In addition, genetic factors play an important role in pathogenesis of VTE. The relationship between common genetic mutations such as factor V Leiden, prothrombin factor II G 20210A, methylenetetrahydrofolate reductase (MTHFR), deficiencies of protein C, protein S, and antithrombin III, and VTE have been reported (2).en10.5152/akd.2012.168info:eu-repo/semantics/openAccessLetter12652752822728734Q3WOS:000308575800022N/A