Cite
Mutations in LMF1 cause combined lipase deficiency and severe hypertriglyceridemia.
MLA
Péterfy, Miklós, et al. “Mutations in LMF1 Cause Combined Lipase Deficiency and Severe Hypertriglyceridemia.” Nature Genetics, vol. 39, no. 12, Dec. 2007, pp. 1483–87. EBSCOhost, https://doi.org/10.1038/ng.2007.24.
APA
Péterfy, M., Ben-Zeev, O., Mao, H. Z., Weissglas-Volkov, D., Aouizerat, B. E., Pullinger, C. R., Frost, P. H., Kane, J. P., Malloy, M. J., Reue, K., Pajukanta, P., & Doolittle, M. H. (2007). Mutations in LMF1 cause combined lipase deficiency and severe hypertriglyceridemia. Nature Genetics, 39(12), 1483–1487. https://doi.org/10.1038/ng.2007.24
Chicago
Péterfy, Miklós, Osnat Ben-Zeev, Hui Z Mao, Daphna Weissglas-Volkov, Bradley E Aouizerat, Clive R Pullinger, Philip H Frost, et al. 2007. “Mutations in LMF1 Cause Combined Lipase Deficiency and Severe Hypertriglyceridemia.” Nature Genetics 39 (12): 1483–87. doi:10.1038/ng.2007.24.