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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Detalles Bibliográficos
Autores principales: Madsen, Daniel Elenius, Hansen, Søren, Gram, Jørgen, Bygum, Anette, Drouet, Christian, Sidelmann, Johannes Jakobsen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4219832/
https://www.ncbi.nlm.nih.gov/pubmed/25369003
http://dx.doi.org/10.1371/journal.pone.0112051

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4219832/
https://www.ncbi.nlm.nih.gov/pubmed/25369003
http://dx.doi.org/10.1371/journal.pone.0112051

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