A point mutation inactivating the sulfonylurea receptor causes the severe form of persistent hyperinsulinemic hypoglycemia of infancy in Finland. by Otonkoski, T, Ammälä, C, Huopio, H, Cote, G, Chapman, J, Cosgrove, K, Ashfield, R, Huang, E, Komulainen, J, Ashcroft, F, Dunne, M, Kere, J, Thomas, P

Altered phenotype of β-cells and other pancreatic cell lineages in patients with diffuse congenital hyperinsulinism in infancy caused by mutations in the ATP-sensitive K-channel by Salisbury, R, Han, B, Jennings, R, Berry, A, Stevens, A, Mohamed, Z, Sugden, S, De Krijger, R, Cross, S, Johnson, P, Newbould, M, Cosgrove, K, Hanley, K, Banerjee, I, Dunne, M, Hanley, N