Rafaelsen, S. H., Ræder, H., Fagerheim, A. K., Knappskog, P., Carpenter, T. O., Johansson, S., & Bjerknes, R. (2013). Exome sequencing reveals FAM20c mutations associated with fibroblast growth factor 23–related hypophosphatemia, dental anomalies, and ectopic calcification. Journal of bone and mineral research, 28(6), 1378-1385. https://doi.org/10.1002/jbmr.1850
Chicago Style (17th ed.) CitationRafaelsen, Silje Hjorth, Helge Ræder, Anne Kristine Fagerheim, Per Knappskog, Thomas O. Carpenter, Stefan Johansson, and Robert Bjerknes. "Exome Sequencing Reveals FAM20c Mutations Associated with Fibroblast Growth Factor 23–related Hypophosphatemia, Dental Anomalies, and Ectopic Calcification." Journal of Bone and Mineral Research 28, no. 6 (2013): 1378-1385. https://doi.org/10.1002/jbmr.1850.
MLA (9th ed.) CitationRafaelsen, Silje Hjorth, et al. "Exome Sequencing Reveals FAM20c Mutations Associated with Fibroblast Growth Factor 23–related Hypophosphatemia, Dental Anomalies, and Ectopic Calcification." Journal of Bone and Mineral Research, vol. 28, no. 6, 2013, pp. 1378-1385, https://doi.org/10.1002/jbmr.1850.