Factor XI gene analysis in thrombophilia and factor XI deficiency

被引：9

作者：

Gerdes, VEA

Kraaijenhagen, RA

Vogels, EWM

Ten Cate, H

Reitsma, PH

机构：

[1] Univ Amsterdam, Acad Med Ctr, Dept Vasc Med, NL-1100 DE Amsterdam, Netherlands

[2] Univ Amsterdam, Acad Med Ctr, Lab Expt Internal Med, NL-1105 AZ Amsterdam, Netherlands

[3] State Univ Limburg Hosp, Dept Internal Med, NL-6201 BX Maastricht, Netherlands

[4] Cardiovasc Res Inst Maastricht, Maastricht, Netherlands

来源：

JOURNAL OF THROMBOSIS AND HAEMOSTASIS | 2004年 / 2卷 / 06期

关键词：

D O I：

10.1111/j.1538-7836.2004.00726.x

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

引用

页码：1015 / 1017

页数：3

共 5 条

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[4] Procoagulant protein levels are differentially increased during human endotoxemia [J].

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[5] Factor XI deficiency in French Basques is caused predominantly by an ancestral Cys38Arg mutation in the factor XI gene [J].

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