AMA
Nocoń-Bohusz J, Wikiera B, Basiak A, Śmigiel R, Noczyńska A. LPL gene mutation as the cause of severe hypertriglyceridemia in the course of ketoacidosis in a patient with newly diagnosed type 1 diabetes mellitus. Pediatric Endocrinology Diabetes and Metabolism. 2015;21(2).
APA
Nocoń-Bohusz, J., Wikiera, B., Basiak, A., Śmigiel, R., & Noczyńska, A. (2015). LPL gene mutation as the cause of severe hypertriglyceridemia in the course of ketoacidosis in a patient with newly diagnosed type 1 diabetes mellitus. Pediatric Endocrinology Diabetes and Metabolism, 21(2).
Chicago
Nocoń-Bohusz, Julita, Beata Wikiera, Aleksander Basiak, Robert Śmigiel, and Anna Noczyńska. 2015. "LPL gene mutation as the cause of severe hypertriglyceridemia in the course of ketoacidosis in a patient with newly diagnosed type 1 diabetes mellitus". Pediatric Endocrinology Diabetes and Metabolism 21 (2).
Harvard
Nocoń-Bohusz, J., Wikiera, B., Basiak, A., Śmigiel, R., and Noczyńska, A. (2015). LPL gene mutation as the cause of severe hypertriglyceridemia in the course of ketoacidosis in a patient with newly diagnosed type 1 diabetes mellitus. Pediatric Endocrinology Diabetes and Metabolism, 21(2).
MLA
Nocoń-Bohusz, Julita et al. "LPL gene mutation as the cause of severe hypertriglyceridemia in the course of ketoacidosis in a patient with newly diagnosed type 1 diabetes mellitus." Pediatric Endocrinology Diabetes and Metabolism, vol. 21, no. 2, 2015.
Vancouver
Nocoń-Bohusz J, Wikiera B, Basiak A, Śmigiel R, Noczyńska A. LPL gene mutation as the cause of severe hypertriglyceridemia in the course of ketoacidosis in a patient with newly diagnosed type 1 diabetes mellitus. Pediatric Endocrinology Diabetes and Metabolism. 2015;21(2).
