Related references
Note: Only part of the references are listed.Sulphonylurea therapy improves cognition in a patient with the V59M KCNJ11 mutation
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KCNJ11 activating mutations are associated with developmental delay, epilepsy and neonatal diabetes syndrome and other neurological features
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Mutations in KCNJ11, which encodes Kir6.2, are a common cause of diabetes diagnosed in the first 6 months of life, with the phenotype determined by genotype
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The identification of a R201H mutation in KCNJ11, which encodes Kir6.2, and successful transfer to sustained-release sulphonylurea therapy in a subject with neonatal diabetes:: evidence for heterogeneity of beta cell function among carriers of the R201H mutation
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Glibenclamide treatment in permanent neonatal diabetes mellitus due to an activating mutation in Kir6.2
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