Hunting for the mutation in inherited thrombophilia

被引：8

作者：

Gomez, K ^{[1
]}

Laffan, MA ^{[1
]}

机构：

[1] Univ London Imperial Coll Sci Technol & Med, Sch Med, Hammersmith Hosp, MRC Clin Sci Ctr, London W12 0NN, England

来源：

BLOOD COAGULATION & FIBRINOLYSIS | 2004年 / 15卷 / 02期

关键词：

thrombophilia; protein C; protein S; antithrombin; mutation;

D O I：

10.1097/00001721-200403000-00002

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

Mutation detection in inherited thrombophilia remains largely confined to the research laboratory. However, there are specific situations when investigating the genetic defect causing thrombophilia can provide additional useful clinical information. This review discusses the value of genetic analysis in the common inherited thrombophilias. (C) 2004 Lippincott Williams Wilkins.

引用

页码：125 / 127

页数：3

共 10 条

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