Plasminogen gene mutation with normal C1 inhibitor hereditary angioedema: Three additional French families

被引：32

作者：

Belbezier, Aude ^{[1
]}

Hardy, Gaelle ^{[2
,3
]}

Marlu, Raphael ^{[2
,4
]}

Defendi, Federica ^{[2
,5
]}

Perard, Chantal Dumestre ^{[2
,5
]}

Boccon-Gibod, Isabelle ^{[1
]}

Launay, David ^{[2
,6
]}

Bouillet, Laurence ^{[1
,2
]}

机构：

[1] Grenoble Univ Hosp, Dept Internal Med, Grenoble, France

[2] CREAK, Natl Reference Ctr Angioedema, Grenoble, France

[3] Grenoble Univ Hosp, Dept Genet Biol, Mol Genet Lab, Grenoble, France

[4] Grenoble Univ Hosp, Lab Hemostasis, Grenoble, France

[5] Grenoble Univ Hosp, Immunol Lab, Grenoble, France

[6] Univ Lille, Dept Internal Med & Clin Immunol, CHU Lille, Lille, France

来源：

ALLERGY | 2018年 / 73卷 / 11期

关键词：

D O I：

10.1111/all.13543

中图分类号：

R392 [医学免疫学];

学科分类号：

100102 ;

摘要：

引用

页码：2237 / 2239

页数：3

共 6 条

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[2]

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[5] A missense mutation in the plasminogen gene, within the plasminogen kringle 3 domain, in hereditary angioedema with normal C1 inhibitor [J].

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[6] A rare mutation in the F12 gene in a patient with ACE inhibitor-induced angioedema [J].

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