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...

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Detaylı Bibliyografya
Yayımlandı:Clin Exp Immunol
Asıl Yazarlar: Deroux, A., Boccon‐Gibod, I., Fain, O., Pralong, P., Ollivier, Y., Pagnier, A., Djenouhat, K., Du‐Thanh, A., Gompel, A., Faisant, C., Launay, D., Bouillet, L.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: John Wiley and Sons Inc. 2016
Konular:
Original Articles
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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