Search
prothrombin gene mutation
Pathology:
- p G20210A mutation associated with coagulopathy
- factor II deficiency if the mutation renders prothrombin non-functional
Related
prothrombin gene
prothrombin genotyping
prothrombin; coagulation factor II; contains: activation peptide fragment 1; activation peptide fragment 2; thrombin light chain; thrombin heavy chain (F2)
General
genetic disease of the blood/bone marrow
Component-of
thrombophilia (hypercoagulability) molecular diagnostic panel