Concepedia
Early Human Development · 2010 · 110 citations · 38 references
38
Mutations in the Sulfonylurea Receptor Gene in Familial Persistent Hyperinsulinemic Hypoglycemia of Infancy
Pamela M. Thomas, Gilbert J. Cote, Nelson Wohllk et al. · Science · 1995 · 816 citations
Medicine, Genetics, Molecular Genetics +16
Hyperinsulinism and Hyperammonemia in Infants with Regulatory Mutations of the Glutamate Dehydrogenase Gene
Charles A. Stanley, Yen K. Lieu, Betty Y.L. Hsu et al. · New England Journal of Medicine · 1998 · 672 citations · Full text
Medicine, Genetics, Molecular Genetics +17
Familial Hyperinsulinism Caused by an Activating Glucokinase Mutation
Benjamin Gläser, Prebakaran Kesavan, Mozhgan Heyman et al. · New England Journal of Medicine · 1998 · 570 citations
Life Sciences, Endocrinology, Genetics +17
Mutation of the pancreatic islet inward rectifier Kir6.2 also leads to familial persistent hyperinsulinemic hypoglycemia of infancy
Paul V. Thomas · Human Molecular Genetics · 1996 · 443 citations
Macrosomia and Hyperinsulinaemic Hypoglycaemia in Patients with Heterozygous Mutations in the HNF4A Gene
Ewan R. Pearson, Sylvia F. Boj, Anna Steele et al. · PLoS Medicine · 2007 · 424 citations · Full text
Medicine, Endocrinology, Genetics +17