- 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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