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
Kir6.2 (KCNJ11) V290M 突变纯合子和杂合子携带者先天性高胰岛素血症和葡萄糖敏感性增高:K(ATP) 通道失活机制及临床治疗
期刊:Diabetes
影响因子:7.5
doi:10.2337/db10-0731
Loechner, Karen J; Akrouh, Alejandro; Kurata, Harley T; Dionisi-Vici, Carlo; Maiorana, Arianna; Pizzoferro, Milena; Rufini, Vittoria; de Ville de Goyet, Jean; Colombo, Carlo; Barbetti, Fabrizio; Koster, Joseph C; Nichols, Colin G