APA (7th ed.) Citation

KJ, L., A, A., HT, K., C, D., A, M., M, P., . . . CG, N. (2011). Congenital hyperinsulinism and glucose hypersensitivity in homozygous and heterozygous carriers of Kir6.2 (KCNJ11) mutation V290M mutation: K(ATP) channel inactivation mechanism and clinical management. Diabetes, 60(1), 209. https://doi.org/10.2337/db10-0731

Chicago Style (17th ed.) Citation

KJ, Loechner, et al. "Congenital Hyperinsulinism and Glucose Hypersensitivity in Homozygous and Heterozygous Carriers of Kir6.2 (KCNJ11) Mutation V290M Mutation: K(ATP) Channel Inactivation Mechanism and Clinical Management." Diabetes 60, no. 1 (2011): 209. https://doi.org/10.2337/db10-0731.

MLA (9th ed.) Citation

KJ, Loechner, et al. "Congenital Hyperinsulinism and Glucose Hypersensitivity in Homozygous and Heterozygous Carriers of Kir6.2 (KCNJ11) Mutation V290M Mutation: K(ATP) Channel Inactivation Mechanism and Clinical Management." Diabetes, vol. 60, no. 1, 2011, p. 209, https://doi.org/10.2337/db10-0731.