Hereditary protein C deficiency with recurrent thrombosis: identification of a missense mutation (C6218T).

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 the last several years, mutations causing PCD have been identified in Western countries and in Japanese...

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שמור ב:
מידע ביבליוגרפי
Main Authors: Song, K. S., Park, Y. S., Choi, C. R., Kim, H. K., Park, Q., Kim, H. S.
פורמט: Artigo
שפה:Inglês
יצא לאור: Korean Academy of Medical Sciences 1998
נושאים:
Research Article
גישה מקוונת:https://ncbi.nlm.nih.gov/pmc/articles/PMC3054489/
https://ncbi.nlm.nih.gov/pubmed/9610620
תגים: הוספת תג
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