METHOD FOR SCREENING PRESENCE OF HEREDITARY DEFECT RELATED TO WEAK ANTICOAGULANT RESPONSE TO THROMBOSIS AND/OR ACTIVATED PROTEIN C

摘要

PROBLEM TO BE SOLVED: To screen presence of hereditary defects related to a weak anticoagulant response to thrombosis and/or activated protein C(APC). SOLUTION: One or more mutations generated to one or more APC splitting and/or bonding parts of the V-th factor and/or the Va-th factor, or the VIII-th factor and/or the VIIIa-th factor in a nucleic acid level or protein level or in both levels are detected with the use of an antibody.