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The hereditary angioedema syndromes
Hereditary angioedema (HAE) is a rare genetic disorder primarily caused by mutations in the SERPING1 gene encoding the C1 inhibitor (C1INH) that leads to plasma deficiency, resulting in recurrent attacks of severe swelling. In the current issue of the JCI, Haslund et al. show that in a subset of pat...
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| Udgivet i: | J Clin Invest |
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| Hovedforfatter: | |
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
American Society for Clinical Investigation
2018
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| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6307950/ https://ncbi.nlm.nih.gov/pubmed/30530986 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1172/JCI125378 |
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