1Otonkoski T, Ammala C, Huopio H, et al.A point mutation inactivating the sulfonylurea receptor cause the severy from of persistent hyperinsulinemic hypoglycemia of infant in Finland. Diabetes, 1999,48: 408-415.
2Glaser B,Thornton P,Otonkosk T,et al.Genetics of disease in childhood UK.Arch Dis Child Fetal Neonatal Ed, 2000,82:79-86.
4Thomas PM, Cote GJ, Hallman DM.Homozygosity mapping, to chromosome 1 1p,of the gene for famililal persistent hyperinsulinemic hypoglycemia of infancy. Am J Hum Genet, 1995,56:416-412.
5Thomas PM,Cote GJ,Wohllk N,et al. Mutations in the sulfonylurea receptor gene in familial hyperinsulinemic hypoglycemia of infancy.Science, 1995,268: 426-429.
6Dunne M J, Kane C, Shepherd RM ,et al. Familial persistent hyperinsulinemic hypoglycemia of infancy and mutations in the sulfonylurea receptor. N EngI J Med, 1997,336:703-706.
7Stantey CA,Lieu YK,Hus BY,et al. Hyperinsulinism and hyperammonemia in infants with regulatory mutations of the glutamate dehydrogenase gene. N EngI J Med, 1998,338:1352-1357.
8Nestorowize A,Inagaki N,Gonol T,et al.A nonsense mutation in the inward rectifier potassium channel gene,KIR6.2,is associated with familial hyperinsulinism. Diabetes, 1997,46:1743-1748.
9Glaser B ,Furth J,Stanley CA,et al. Intragenic singal nucleotide polymorphism haplotype analysis of SURI mutations in familial hypeinsulinsim.Hum Murat, 1999,14:23-29.
10Stanley C.Hyperinsulinism in infants and children. Pediatr Clin Nor Am, 1997,44: 363-374.
