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
收藏
页码：432 / 432
页数：1
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