Björkqvist, J., de Maat, S., Lewandrowski, U., Di Gennaro, A., Oschatz, C., Schönig, K., . . . Renné, T. (2015). Defective glycosylation of coagulation factor XII underlies hereditary angioedema type III. Journal of Clinical Investigation, 125(8), 3132. https://doi.org/10.1172/JCI77139
Chicago Style (17th ed.) CitationBjörkqvist, Jenny, et al. "Defective Glycosylation of Coagulation Factor XII Underlies Hereditary Angioedema Type III." Journal of Clinical Investigation 125, no. 8 (2015): 3132. https://doi.org/10.1172/JCI77139.
MLA (9th ed.) CitationBjörkqvist, Jenny, et al. "Defective Glycosylation of Coagulation Factor XII Underlies Hereditary Angioedema Type III." Journal of Clinical Investigation, vol. 125, no. 8, 2015, p. 3132, https://doi.org/10.1172/JCI77139.