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Diagnosis and treatment of hereditary angioedema with normal C1 inhibitor
Until recently it was assumed that hereditary angioedema is a disease that results exclusively from a genetic deficiency of the C1 inhibitor. In 2000, families with hereditary angioedema, normal C1 inhibitor activity and protein in plasma were described. Since then numerous patients and families wit...
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
BioMed Central
2010
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| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2919521/ https://ncbi.nlm.nih.gov/pubmed/20667118 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1710-1492-6-15 |
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