Description
Coagulation factor VIII, or antihemophilic globulin, is one of the factors of the intrinsic pathway of the plasma coagulation cascade. Its deficiency is the cause of the hereditary disease hemophilia A, the main manifestation of which is a predisposition to increased bleeding tendency and spontaneous and prolonged recurrent bleeding.
Period of execution
Within 9 days. The specified time does not include the day of biomaterial collection
Biomaterial type