Treatment of patients with hereditary angioedema with the c.988A>G (p.Lys330Glu) variant in the plasminogen gene | Orphanet Journal of Rare Diseases | Full Text

Treatment of patients with hereditary angioedema with the c.988A>G (p.Lys330Glu) variant in the plasminogen gene | Orphanet Journal of Rare Diseases | Full Text

Treatment of patients with hereditary angioedema with the c.988A>G (p.Lys330Glu) variant in the plasminogen gene

Hereditary angioedema (HAE) in patients with normal C1 inhibitor (C1-INH) and the c.988A > G (p.Lys330Glu; p.K330E) variant in the plasminogen gene (HAE-PLG) is associated with skin swellings, abdominal pain a...

Authors:Konrad Bork, Karin Wulff, Guenther Witzke, Thomas Machnig and Jochen Hardt

Citation:Orphanet Journal of Rare Diseases 2020 15:52

Content type:Research

Published on: 17 February 2020

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