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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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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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