Plasminogen gene mutation with normal C1 inhibitor hereditary angioedema: Three additional French families
Allergy
.
2018 Nov;73(11):2237-2239.
doi: 10.1111/all.13543.
Epub 2018 Jul 26.
Authors
Aude Belbézier
1
,
Gaelle Hardy
2
3
,
Raphael Marlu
2
4
,
Federica Defendi
2
5
,
Chantal Dumestre Perard
2
5
,
Isabelle Boccon-Gibod
1
2
,
David Launay
2
6
,
Laurence Bouillet
1
2
Affiliations
1
Department of Internal Medicine, Grenoble University Hospital, Grenoble, France.
2
National Reference Centre for Angioedema, CREAK, Grenoble, France.
3
Laboratory of Molecular Genetics, Department of Genetic Biology, Grenoble University Hospital, Grenoble, France.
4
Laboratory of Hemostasis, Grenoble University Hospital, Grenoble, France.
5
Laboratory of Immunology, Grenoble University Hospital, Grenoble, France.
6
Department of Internal Medicine and Clinical Immunology, CHU Lille, Univ. Lille, Lille, France.
PMID:
29952006
DOI:
10.1111/all.13543
No abstract available
Publication types
Letter
Comment
MeSH terms
Angioedemas, Hereditary*
Complement C1 Inhibitor Protein / genetics
Humans
Mutation
Plasminogen
Substances
Complement C1 Inhibitor Protein
Plasminogen