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...

全面介紹

Na minha lista:
書目詳細資料
發表在:Clin Exp Immunol
Main Authors: 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.
格式: Artigo
語言:Inglês
出版: John Wiley and Sons Inc. 2016
主題:
Original Articles
在線閱讀: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
標簽: 添加標簽
沒有標簽, 成為第一個標記此記錄!

相似書籍