葡萄糖激酶
先证者
青少年成熟型糖尿病
突变
无症状的
外显子
糖尿病
内科学
遗传学
内分泌学
医学
人口
基因突变
基因
杂合子优势
生物
基因型
环境卫生
作者
Pingping Hong,Bingjie Guo,Li Lin,Xihua Lin,Jiaheng Zhou
出处
期刊:PubMed
日期:2019-04-25
卷期号:48 (2): 200-203
标识
DOI:10.3785/j.issn.1008-9292.2019.04.12
摘要
Maturity onset diabetes of the young (MODY) is a monogenic autosomal dominant inherited disease. Its clinical manifestations are asymptomatic with slightly elevated fasting blood glucose and few complications. This paper reports a novel mutation W257R in glucokinase (GCK) gene from a Chinese patient with MODY. Heterozygous mutation c.769T>C (p.W257R) in exon 7 of GCK gene (Chr744187343) was found in the proband, her father and brother. This W257R mutation was first reported in Chinese population.
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