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
收藏
页码：2237 / 2239
页数：3
相关论文
共 6 条
  • [1] Mutation of the angiopoietin-1 gene (ANGPT1) associates with a new type of hereditary angioedema
    Bafunno, Valeria
    Firinu, Davide
    D'Apolito, Maria
    Cordisco, Giorgia
    Loffredo, Stefania
    Leccese, Angelica
    Bova, Maria
    Barca, Maria Pina
    Santacroce, Rosa
    Cicardi, Marco
    Del Giacco, Stefano
    Margaglione, Maurizio
    [J]. JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2018, 141 (03) : 1009 - 1017
  • [2] Binkley KE, 2000, J ALLERGY CLIN IMMUN, V106, P546
  • [3] Hereditary angioedema with a mutation in the plasminogen gene
    Bork, K.
    Wulff, K.
    Steinmueller-Magin, L.
    Braenne, I.
    Staubach-Renz, P.
    Witzke, G.
    Hardt, J.
    [J]. ALLERGY, 2018, 73 (02) : 442 - 450
  • [4] Hereditary angioedema with normal C1 inhibitor and factor XII mutation: a series of 57 patients from the French National Center of Reference for Angioedema
    Deroux, A.
    Boccon-Gibod, I.
    Fain, O.
    Pralong, P.
    Ollivier, Y.
    Pagnier, A.
    Djenouhat, K.
    Du-Thanh, A.
    Gompel, A.
    Faisant, C.
    Launay, D.
    Bouillet, L.
    [J]. CLINICAL AND EXPERIMENTAL IMMUNOLOGY, 2016, 185 (03) : 332 - 337
  • [5] A missense mutation in the plasminogen gene, within the plasminogen kringle 3 domain, in hereditary angioedema with normal C1 inhibitor
    Dewald, Georg
    [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2018, 498 (01) : 193 - 198
  • [6] A rare mutation in the F12 gene in a patient with ACE inhibitor-induced angioedema
    Veronez, Camila Lopes
    Serpa, Faradiba Sarquis
    Pesquero, Joao Bosco
    [J]. ANNALS OF ALLERGY ASTHMA & IMMUNOLOGY, 2017, 118 (06) : 743 - 745
1