Factor II prothrombin mutation
This test is done to identify a mutation in the prothrombin (Factor II) gene that can increase the risk of abnormal blood clot formation. It helps assess inherited risk for conditions such as deep vein thrombosis or pulmonary embolism, especially in individuals with a personal or family history of clotting disorders.
Al Arabi Laboratory & Radiology
Al Jazira Al Arabiya Street, Doha, Qatar
Al Jazira Al Arabiya Street Doha, Qatar