C1 Inhibitor
C1-INH-HAE
SERPING1 gene
angioedema
genetic variation
hereditary–diagnosis
serpin function
serpinopathy
Journal
Frontiers in allergy
ISSN: 2673-6101
Titre abrégé: Front Allergy
Pays: Switzerland
ID NLM: 9918227355906676
Informations de publication
Date de publication:
2022
2022
Historique:
received:
14
12
2021
accepted:
16
02
2022
entrez:
12
8
2022
pubmed:
13
8
2022
medline:
13
8
2022
Statut:
epublish
Résumé
Hereditary angioedema with C1 Inhibitor deficiency (C1-INH-HAE) is caused by a constellation of variants of the
Identifiants
pubmed: 35958943
doi: 10.3389/falgy.2022.835503
pmc: PMC9361472
doi:
Types de publication
Journal Article
Review
Langues
eng
Pagination
835503Informations de copyright
Copyright © 2022 Drouet, López-Lera, Ghannam, López-Trascasa, Cichon, Ponard, Parsopoulou, Grombirikova, Freiberger, Rijavec, Veronez, Pesquero and Germenis.
Déclaration de conflit d'intérêts
AGh was employed by KininX SAS. FP and AGe were employed by CeMIA SA. The remaining authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
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