Andrejević, S., Korošec, P., Šilar, M., Košnik, M., Mijanović, R., Bonači-Nikolić, B., & Rijavec, M. (2015). Hereditary Angioedema Due to C1 Inhibitor Deficiency in Serbia: Two Novel Mutations and Evidence of Genotype-Phenotype Association. Public Library of Science.

Andrejević, Slađana, Peter Korošec, Mira Šilar, Mitja Košnik, Radovan Mijanović, Branka Bonači-Nikolić, and Matija Rijavec. Hereditary Angioedema Due to C1 Inhibitor Deficiency in Serbia: Two Novel Mutations and Evidence of Genotype-Phenotype Association. Public Library of Science, 2015.

Andrejević, Slađana, et al. Hereditary Angioedema Due to C1 Inhibitor Deficiency in Serbia: Two Novel Mutations and Evidence of Genotype-Phenotype Association. Public Library of Science, 2015.