“…Nine genes have been identified and classified within the potassium channelopathies (ABCC8, KCNJ11) and metabolic disorders (GLUD1, GCK, HNF4A, HNF1A, SLC16A1, UCP2, HADH) [47,52]. Genetic defect mutations involving the ABCC8/KCNJ11 genes, which encode the SUR1/Kir 6.2 components of the ATP-sensitive potassium channels (K ATP ) in pancreatic beta cells, are the most common [13,27]. In normal cells, the K ATP channels remain open or closed in response to variation in blood glucose levels, which leads to changes in the action potential of the cell membrane.…”