APA (7th ed.) Citation

Kay, L., Tokarska-Schlattner, M., & Bugert, P. (2017). Creatine kinase in human erythrocytes: A genetic anomaly reveals presence of soluble brain-type isoform. Blood cells, molecules & diseases, 64, . https://doi.org/10.1016/j.bcmd.2017.03.008

Chicago Style (17th ed.) Citation

Kay, Laurence, Malgorzata Tokarska-Schlattner, and Peter Bugert. "Creatine Kinase in Human Erythrocytes: A Genetic Anomaly Reveals Presence of Soluble Brain-type Isoform." Blood Cells, Molecules & Diseases 64 (2017). https://doi.org/10.1016/j.bcmd.2017.03.008.

MLA (9th ed.) Citation

Kay, Laurence, et al. "Creatine Kinase in Human Erythrocytes: A Genetic Anomaly Reveals Presence of Soluble Brain-type Isoform." Blood Cells, Molecules & Diseases, vol. 64, 2017, https://doi.org/10.1016/j.bcmd.2017.03.008.