Loechner, K. J., Akrouh, A., Kurata, H. T., Dionisi-Vici, C., Maiorana, A., Pizzoferro, M., . . . Nichols, C. G. (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. American Diabetes Association.
Chicago Style CitationLoechner, Karen J., 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. American Diabetes Association, 2011.
MLA CitationLoechner, Karen J., 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. American Diabetes Association, 2011.