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Article

GCK mutations in Chinese MODY2 patients: a family pedigree report and review of Chinese literature.

Journal of pediatric endocrinology & metabolism : JPEM - 1 Aug 2016

Ping Xiao Yu, Hua Xu Xiao, Lan Fang Yan, Jiang LiQiong, Chen Chun, Liang Li, Lin Wang Chun

Abstract excerpt

BACKGROUND: Maturity-onset diabetes of the young type 2 (MODY2) is caused by mutations in the glucokinase (GCK) gene and is rare in the Chinese population. We report three Chinese families with MODY2 and the sequencing of the GCK gene. METHODS: Three unrelated Chinese families with MODY2 and their pedigrees were investigated. In Family 1, the proband was a 7-year-old girl with impaired fasting glucose (IFG) and...

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Source

Identifiers

PMID: 27269892
DOI: 10.1515/jpem-2015-0354

Genes

GCK

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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