MISSENSE GLUCOKINASE MUTATION IN MATURITY-ONSET DIABETES OF THE YOUNG AND MUTATION SCREENING IN LATE-ONSET DIABETES

被引:120
|
作者
STOFFEL, M
PATEL, P
LO, YMD
HATTERSLEY, AT
LUCASSEN, AM
PAGE, R
BELL, JI
BELL, GI
TURNER, RC
WAINSCOAT, JS
机构
[1] UNIV CHICAGO,HOWARD HUGHES MED INST,CHICAGO,IL 60637
[2] RADCLIFFE INFIRM,DIABET RES LABS,OXFORD OX2 6HE,ENGLAND
[3] JOHN RADCLIFFE HOSP,INST MOLEC MED,OXFORD OX3 9DU,ENGLAND
[4] JOHN RADCLIFFE HOSP,NUFFIELD DEPT PATHOL & BACTERIOL,OXFORD OX3 9DU,ENGLAND
[5] JOHN RADCLIFFE HOSP,DEPT HAEMATOL,OXFORD OX3 9DU,ENGLAND
[6] UNIV CHICAGO,DEPT BIOCHEM & MOLEC BIOL,CHICAGO,IL 60637
[7] UNIV CHICAGO,DEPT MED,CHICAGO,IL 60637
基金
英国惠康基金;
关键词
D O I
10.1038/ng1092-153
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
We describe a codon 299 mutation in the glucokinase gene in a British pedigree with maturity-onset diabetes of the young (MODY) resulting in a substitution of glycine to arginine. One out of fifty patients diagnosed with classical late-onset type 2 diabetes mellitus was also found to have this mutation. All nine relatives of this patient who have inherited the mutation have type 2 diabetes, although six others without the mutation are also present with diabetes. The discovery that glucokinase mutations can cause MODY and was also found in ten affected members of a pedigree with type 2 diabetes in which MODY had not previously been considered indicates that diagnosis based on molecular pathology will be helpful in understanding the aetiology of type 2 diabetes.
引用
收藏
页码:153 / 156
页数:4
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