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Article

Novel deletion mutation in the glucokinase gene from a korean man with GCK-MODY phenotype and situs inversus.

Diabetes research and clinical practice - 1 Sept 2018

Cho Yun Kyung, Cho Eun-Hee, Choi Hoon Sung, Kim Sang-Wook

Abstract excerpt

A novel mutation in intron 9-exon 10 boundary of the GCK gene was detected in a male patient with clinical features of GCK-MODY and situs inversus. This case highlights the value of sequencing the GCK gene in individuals with GCK-MODY phenotype and no family history of monogenic diabetes.

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Source

Identifiers

PMID: 30086370
DOI: 10.1016/j.diabres.2018.07.036

Genes

GCK

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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