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Case Reports
. 2005 May;48(5):1029-31.
doi: 10.1007/s00125-005-1731-5. Epub 2005 Apr 19.

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

T Klupa, E L Edghill, J Nazim, J Sieradzki, S Ellard, A T Hattersley, M T Malecki
Case Reports

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

T Klupa et al. Diabetologia. 2005 May.
No abstract available

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References

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