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Glucokinase gene mutations (MODY 2) in Asian Indians.

Diabetes technology & therapeutics - 1 Mar 2014

Kanthimathi Sekar, Jahnavi Suresh, Balamurugan Kandasamy, Ranjani Harish, Sonya Jagadesan, Goswami Soumik, Chowdhury Subhankar, Mohan Viswanathan, Radha Venkatesan

Abstract excerpt

BACKGROUND AND AIM: Heterozygous inactivating mutations in the glucokinase (GCK) gene cause a hyperglycemic condition termed maturity-onset diabetes of the young (MODY) 2 or GCK-MODY. This is characterized by mild, stable, usually asymptomatic, fasting hyperglycemia that rarely requires pharmacological intervention. The aim of the present study was to screen for GCK gene mutations in Asian Indian subjects with...

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Identifiers

PMID: 24405491
DOI: 10.1089/dia.2013.0244

Genes

GCK

Variants

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026. Manifest publication-graph-cohort-2026-09-05.1.

Source receipt: pubmed, retrieved 5 Sept 2026.

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