Table 1.
Clinical data of Serbian patients with C1-INH-HAE.
Fig 1.
Mutations identified in the SERPING1 gene in Serbian families with hereditary angioedema due to C1 inhibitor deficiency.
Boxes showing the novel mutations identified are shaded in grey.
Table 2.
Mutations found in Serbian patients with C1-INH-HAE.
Table 3.
Genotype-phenotype association analysis in C1-INH-HAE patients from Serbia.