Secreted Phospholipases A2 in Hereditary Angioedema With C1-Inhibitor Deficiency
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DOI: 10.3389/fimmu.2018.01721
Abstract: Background Hereditary angioedema (HAE) caused by deficiency (type I) or dysfunction (type II) of the C1 inhibitor protein (C1-INH-HAE) is a disabling, potentially fatal condition characterized by recurrent episodes of swelling. We have recently found… read more here.
Keywords: hgiia; inhibitor; permeability; inh hae ... See more keywords