Presence of C1-Inhibitor Polymers in a Subset of Patients Suffering from Hereditary Angioedema

Hereditary angioedema (HAE) is a potentially life-threatening disease caused by mutations in the gene encoding the serine protease inhibitor (serpin) C1 inhibitor (C1-inh). The mutations cause decreased functional plasma levels of C1-inh, which triggers unpredictable recurrent edema attacks. Subject...

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Veröffentlicht in:PLoS One
Hauptverfasser: Madsen, Daniel Elenius, Hansen, Søren, Gram, Jørgen, Bygum, Anette, Drouet, Christian, Sidelmann, Johannes Jakobsen
Format: Artigo
Sprache:Inglês
Veröffentlicht: Public Library of Science 2014
Schlagworte:
Research Article
Online Zugang:https://ncbi.nlm.nih.gov/pmc/articles/PMC4219832/
https://ncbi.nlm.nih.gov/pubmed/25369003
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0112051
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