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

    Speletas, M.; Szilágyi, Á; Csuka, D.; Koutsostathis, N.; Psarros, F.; Moldovan, D.; Magerl, M.; Kompoti, M.; Varga, L.; Maurer, M.; Farkas, H.; Germenis, A. E. (2015)
    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 ...