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Disease-modifying factors in hereditary angioedema: an RNA expression-based screening
BACKGROUND: Hereditary Angioedema due to C1-Inhibitor deficiency (HAE types I and II) is a monogenic disease characterized by sudden, self-limited episodes of cutaneous and mucosal swelling due to local deregulation of vascular permeability. Despite its monogenic pattern of inheritance, HAE exhibits...
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| Autori principali: | , , , , |
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| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
BioMed Central
2013
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3671971/ https://ncbi.nlm.nih.gov/pubmed/23688356 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1750-1172-8-77 |
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