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：57

作者：

Klupa, T

Edghill, E

Nazim, J

Sieradzki, J

Ellard, S

Hattersley, A

Malecki, M

机构：

[1] Jagiellonian Univ, Dept Metab Dis, Coll Med, PL-31501 Krakow, Poland

[2] Peninsula Med Sch, Inst Biomed & Clin Sci, Exeter, Devon, England

[3] Jagiellonian Univ, Coll Med, Polish Amer Childrens Hosp, Dept Paediat Endocrinol, Krakow, Poland

来源：

DIABETOLOGIA | 2005年 / 48卷 / 05期

基金：

英国惠康基金;

关键词：

D O I：

10.1007/s00125-005-1731-5

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

引用

页码：1029 / 1031

页数：3

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