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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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| 出版年: | PLoS One |
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| 主要な著者: | , , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Public Library of Science
2014
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| 主題: | |
| オンライン･アクセス: | 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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