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. - Loechner KJ; Akrouh A; Kurata HT; Dionisi-Vici C; Maiorana A; Pizzoferro M; Rufini V; de Ville de Goyet J; Colombo C; Barbetti F; Koster JC; Nichols CG (Diabetes, 2011)