| Literature DB >> 31309759 |
Pingping Hong1, Bingjie Guo1, Li Lin1, Xihua Lin1, Jiaqiang Zhou1.
Abstract
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.Entities:
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Year: 2019 PMID: 31309759 PMCID: PMC8800652 DOI: 10.3785/j.issn.1008-9292.2019.04.12
Source DB: PubMed Journal: Zhejiang Da Xue Xue Bao Yi Xue Ban ISSN: 1008-9292