Listar por tema "F12-46C/T polymorphism"
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F12-46C/T polymorphism as modifier of the clinical phenotype of hereditary angioedema
(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 ...