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

被引:0
|
作者
T. Klupa
E. L. Edghill
J. Nazim
J. Sieradzki
S. Ellard
A. T. Hattersley
M. T. Malecki
机构
[1] Jagiellonian University,Department of Metabolic Diseases, Medical College
[2] Peninsula Medical School,Institute of Biomedical and Clinical Science
[3] Jagiellonian University,Department of Paediatric Endocrinology, Polish
来源
Diabetologia | 2005年 / 48卷
关键词
Beta Cell; Sulphonylurea; Glipizide; Continuous Glucose Monitoring; Neonatal Diabetes;
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学科分类号
摘要
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页码:1029 / 1031
页数:2
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