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

Springer Science and Business Media LLC - Tập 48 - Trang 1029-1031 - 2005
T. Klupa1, E. L. Edghill2, J. Nazim3, J. Sieradzki1, S. Ellard2, A. T. Hattersley2, M. T. Malecki1
1Department of Metabolic Diseases, Medical College, Jagiellonian University, Krakow, Poland.
2Institute of Biomedical and Clinical Science, Peninsula Medical School, Exeter, UK
3Department of Paediatric Endocrinology, Polish-American Children’s Hospital, Medical College, Jagiellonian University, Krakow, Poland

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Springer Science and Business Media LLC

Tập 48

1029-1031

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