Cite

Hereditary angioedema due to C1-inhibitor deficiency in Macedonia: clinical characteristics, novel <italic>SERPING1</italic> mutations and genetic factors modifying the clinical phenotype.

MLA

Grivčeva-Panovska, Vesna, et al. “Hereditary Angioedema Due to C1-Inhibitor Deficiency in Macedonia: Clinical Characteristics, Novel SERPING1 Mutations and Genetic Factors Modifying the Clinical Phenotype.” Annals of Medicine, vol. 50, no. 3, May 2018, pp. 269–76. EBSCOhost, https://doi.org/10.1080/07853890.2018.1449959.



APA

Grivčeva-Panovska, V., Košnik, M., Korošec, P., Andrejević, S., Karadža-Lapić, L., & Rijavec, M. (2018). Hereditary angioedema due to C1-inhibitor deficiency in Macedonia: clinical characteristics, novel SERPING1 mutations and genetic factors modifying the clinical phenotype. Annals of Medicine, 50(3), 269–276. https://doi.org/10.1080/07853890.2018.1449959



Chicago

Grivčeva-Panovska, Vesna, Mitja Košnik, Peter Korošec, Slađana Andrejević, Ljerka Karadža-Lapić, and Matija Rijavec. 2018. “Hereditary Angioedema Due to C1-Inhibitor Deficiency in Macedonia: Clinical Characteristics, Novel SERPING1 Mutations and Genetic Factors Modifying the Clinical Phenotype.” Annals of Medicine 50 (3): 269–76. doi:10.1080/07853890.2018.1449959.