Prothrombin deficiency caused by compound heterozygosity for two novel mutations in the prothrombin gene associated with a bleeding tendency

被引：1
|
作者：
Stanchev, H
Philips, M
Villoutreix, BO
Aksglaede, L
Lethagen, S
Thorsen, S
机构：
[1] Rigshosp, Ctr Diagnost, Dept Clin Biochem, DK-2100 Copenhagen O, Denmark
[2] Dept Pediat, Naestved, Denmark
[3] Copenhagen Univ Hosp, Dept Clin Biochem, Rigshosp, Copenhagen, Denmark
[4] Univ Paris 05, INSERM, U648, Sch Pharm, Paris, France
[5] Copenhagen Univ Hosp, Rigshosp, Dept Pediat, Haemophilia Ctr, Copenhagen, Denmark
[6] Malmo Univ Hosp, Univ Lund, Dept Coagulat Disorders, Malmo, Sweden
来源：
THROMBOSIS AND HAEMOSTASIS | 2006年 / 95卷 / 01期
关键词：
D O I：
暂无
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
引用
收藏
页码：195 / 198
页数：4
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