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

Karen J. Loechner, Alejandro Akrouh, Harley T. Kurata, Carlo Dionisi-Vici, Arianna Maiorana, Milena Pizzoferro, Vittoria Rufini, Jean De Ville De Goyet, Carlo Colombo, Fabrizio Barbetti, Joseph C. Koster, Colin G. Nichols

Research output: Contribution to journal › Article › peer-review

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