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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.
Klupa T, Edghill EL, Nazim J, Sieradzki J, Ellard S, Hattersley AT, Malecki MT. Klupa T, et al. Diabetologia. 2005 May;48(5):1029-31. doi: 10.1007/s00125-005-1731-5. Epub 2005 Apr 19. Diabetologia. 2005. PMID: 15838686 No abstract available.