- Activated Protein C Anticoagulant System Dysfunction and Thrombophilia in Asia
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Hamasaki N, Kuma H, Tsuda H
- KMID: 1781292
- Ann Lab Med.
- 2013 Jan;33(1):8-13.
- doi: 10.3343/alm.2013.33.1.8
Thrombophilia that is common among Caucasians is caused by genetic polymorphisms of coagulation factor V Leiden (R506Q) and prothrombin G20210A. Unlike that in Caucasians, thrombophilia that is common in the... -
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- Hereditary protein C deficiency with recurrent thrombosis: identification of a missense mutation (C6218T)
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Song KS, Park YS, Choi CR, Kim HK, Park Q, Kim HS
- KMID: 1064967
- J Korean Med Sci.
- 1998 Apr;13(2):186-190.
- doi: 10.3346/jkms.1998.13.2.186
Protein C is the central component of a major anti-thrombotic regulatory system and individuals with hereditary protein C deficiency (PCD) tend to have an increased risk of thromboembolism. During... -
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- A molecular model of a point mutation (Val297Met) in the serine protease domain of protein C
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Song KS, Park YS, Choi JR, Kim HK, Park Q
- KMID: 755027
- Exp Mol Med.
- 1999 Mar;31(1):47-51.
A heterozygous GTG to ATG (Val297Met) mutation was detected in a patient with inherited protein C deficiency and deep vein thrombosis. Cosegregation of the mutation with protein C deficiency was observed through... -
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