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458 Differences of Complement Activation Profile between Type I and Type II of Hereditary Angioedema Due to C1-inhibitor Deficiency

BACKGROUND: In hereditary angioedema (HAE), diverse mutations in the C1-inhibitor gene may produce either normal C1-inhibitor protein in insufficient quantities (HAE type I), or a dysfunctional protein in normal or even excessive amounts (HAE type II). Previously, we have found strong association be...

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Detaylı Bibliyografya
Asıl Yazarlar: Csuka, Dorottya, Kelemen, Zsuzsanna, Varga, Lilian, Füst, George, Farkas, Henriette
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: World Allergy Organization Journal 2012
Konular:
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC3513152/
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1097/01.WOX.0000411573.74196.57
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