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F12-46C/T polymorphism as modifier of the clinical phenotype of hereditary angioedema

F12-46C/T polymorphism as modifier of the clinical phenotype of hereditary angioedema

by mm-red | Jul 30, 2020

The factors influencing the heterogeneous clinical manifestation of hereditary angioedema due to C1-INH deficiency (C1-INH-HAE) represent one of the oldest unsolved problems of the disease. Considering that factor XII (FXII) levels may affect bradykinin production, we...
F12-46C/T polymorphism as modifier of the clinical phenotype of hereditary angioedema

Genetic determinants of C1 inhibitor deficiency angioedema age of onset

by mm-red | Jul 29, 2020

Background: In view of the large heterogeneity in the clini- cal presentation of hereditary angioedema due to C1 inhibitor deficiency (C1-INH-HAE), great efforts are being made to- wards detecting measurable biological determinants of disease severity that can help to...

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