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Hereditary angioedema with normal C1 inhibitor and factor XII mutation: a series of 57 patients from the French National Center of Reference for Angioedema
Hereditary angioedema (HAE) is a rare disease associated with either a quantitative or qualitative deficiency in C1‐inhibitor (C1‐INH) or normal C1‐INH. HAE with normal C1‐INH is associated in 20% of cases with mutations in the gene for factor XII (FXII) or FXII‐HAE. A recent review described 41 fam...
Kaydedildi:
| Yayımlandı: | Clin Exp Immunol |
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| Asıl Yazarlar: | , , , , , , , , , , , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
John Wiley and Sons Inc.
2016
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4991515/ https://ncbi.nlm.nih.gov/pubmed/27271546 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/cei.12820 |
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