Hereditary angioedema with normal C1Inhibitor and factor XII mutation: a French cohort

被引：0

作者：

Boccon-Gibod, I ^{[1
,2
]}

Bouillet, L. ^{[1
,2
]}

Gompel, A. ^{[2
,3
]}

Fain, O. ^{[2
,4
]}

Du-Thanh, A. ^{[2
,5
]}

Raison-Peyron, N. ^{[2
,5
]}

Ollivier, Y. ^{[2
,6
]}

Gayet, S. ^{[2
,7
]}

Pralong, P. ^{[8
]}

Djenouhat, K. ^{[9
]}

Kirk, R. ^{[10
]}

机构：

[1] Grenoble Univ Hosp, Grenoble, France

[2] Natl Reference Ctr Angioedema, Grenoble, France

[3] Port Royal Cochin, APHP, Paris, France

[4] Jean Verdier Hosp, APHP, Bondy, France

[5] St Eloi Univ Hosp, Montpellier, France

[6] Cote Nacre Univ Hosp, Caen, France

[7] Concept Hosp, Ap Hm, Marseille, France

[8] Hop Lyon Sud, Lyon, France

[9] Inst Pasteur, Algiers, Algeria

[10] Princess Alexandra Hosp NHS Trust, Dept Child Hlth, Harlow, Essex, England

来源：

ALLERGY | 2013年 / 68卷

关键词：

D O I：

暂无

中图分类号：

R392 [医学免疫学];

学科分类号：

100102 ;

摘要：

引用

页码：432 / 432

页数：1

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