Severe factor XI deficiency caused by compound heterozygosity

被引：7

作者：

Dai, L ^{[1
]}

Mitchell, M

Carson, P

Creagh, D

Cutler, J

Savidge, G

Alhaq, A

机构：

[1] St Thomas Hosp, Ctr Haemostasis & Thrombosis, Haemophilia Reference Ctr, London, England

[2] Royal Cornwall Hosp, Dept Haematol, Truro, Cornwall, England

来源：

BRITISH JOURNAL OF HAEMATOLOGY | 2004年 / 125卷 / 06期

关键词：

factor XI deficiency; mutation; compound heterozygosity;

D O I：

10.1111/j.1365-2141.2004.04979.x

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

引用

页码：817 / 818

页数：3

共 6 条

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[4] IDENTIFICATION OF 2 NOVEL MUTATIONS IN NON-JEWISH FACTOR-XI DEFICIENCY [J].

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[5] The Human Gene Mutation Database [J].

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[6] 6 POINT MUTATIONS THAT CAUSE FACTOR-XI DEFICIENCY [J].

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