Update of mutations in the genes encoding the pancreatic beta-cell K(ATP) channel subunits Kir6.2 (KCNJ11) and sulfonylurea receptor 1 (ABCC8) in diabetes mellitus and hyperinsulin... by Flanagan, SE, Clauin, S, Bellanné-Chantelot, C, de Lonlay, P, Harries, L, Gloyn, A, Ellard, S

Update on mutations in glucokinase (GCK), which cause maturity-onset diabetes of the young, permanent neonatal diabetes, and hyperinsulinemic hypoglycemia. by Osbak, K, Colclough, K, Saint-Martin, C, Beer, N, Bellanné-Chantelot, C, Ellard, S, Gloyn, A

KCNJ11 activating mutations are associated with developmental delay, epilepsy and neonatal diabetes syndrome and other neurological features. by Gloyn, A, Diatloff-Zito, C, Edghill, E, Bellanné-Chantelot, C, Nivot, S, Coutant, R, Ellard, S, Hattersley, A, Robert, J