A method for screening for the presence of a genetic defect associated with thrombosis and / or poor anticoagulant response to activated protein C.

摘要

METHOD TO INVESTIGATE THE GENETIC DEFECT PRESENCE OF ASSOCIATE WITH THROMBOSIS AND / OR RESPONSE TO ANTICOAGULANT insufficient to activated protein C (APC). The method is directed to the detection of one or more mutations IN ONE OR MORE OF THE SPACE FOR DIVISION AND / OR LINK APC FACTOR VY / or Factor Va or Factor VIII and / or FACTOR VIIIA IN NUCLEIC ACID OR LEVEL PROTEIN OR BOTH.