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Familial hyperglycemia due to mutations in glucokinase. Definition of a subtype of diabetes mellitus
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Identification of 14 new glucokinase mutations and description of the clinical profile of 42 MODY-2 families
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Glucokinase (GCK) mutations in hyper- And hypoglycemia: Maturity-onset diabetes of the young, permanent neonatal diabetes, and hyperinsulinemia of infancy
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Mutations in the hepatocyte nuclear factor-1alpha gene in maturity-onset diabetes of the young (MODY3)
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Mutation in hepatocyte nuclear factor-1 beta gene (TCF2) associated with MODY
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Mutations in NEUROD1 are associated with the development of type 2 diabetes mellitus
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Activating mutations in the gene encoding the ATP-sensitive potassium-channel subunit Kir6.2 and permanent neonatal diabetes
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Activating mutations in the ABCC8 gene in neonatal diabetes mellitus
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Permanent neonatal diabetes due to mutations in KCNJ11 encoding Kir6.2: Patient characteristics and initial response to sulfonylurea therapy
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Neonatal diabetes in a child positive for islet cell antibodies at onset and Kir6.2 activating mutation
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