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Article

Genetic testing for glucokinase mutations in clinically selected patients with MODY: a worthwhile investment.

Swiss medical weekly - 11 Jun 2005

Schnyder Sabine, Mullis Primus E, Ellard Sian, Hattersley Andrew T, Flück Christa E

Abstract excerpt

The differential diagnosis for children with diabetes includes a group of monogenic diabetic disorders known as maturity-onset diabetes of the young (MODY). So far, six underlying gene defects have been identified. The most common subtypes are caused by mutations in the genes encoding the transcr...

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Share to Child, Preschool
Share to Diabetes Mellitus, Type 2
Share to Diagnosis, Differential

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Share to Genetic Testing

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Share to Hepatocyte Nuclear Factor 1-alpha

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Source

Identifiers

PMID: 16059790
DOI: 10.4414/smw.2005.11030

Genes

GCK

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-16059790-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

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Genetic testing for glucokinase mutations in clinically selected patients with MODY: a worthwhile investment.PMID 16059790Read ↗

Analysis of mutations in the glucokinase gene in people clinically characterized as MODY2 without a family history of diabetes.Semantic proximity Read ↗

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A review of maturity onset diabetes of the young (MODY) and challenges in the management of glucokinase-MODY.Semantic proximity Read ↗

Who should have genetic testing for maturity-onset diabetes of the young?Semantic proximity Read ↗

Maturity-onset diabetes of the young (MODY): an update.Semantic proximity Read ↗

Current views on etiology, diagnosis, epidemiology and gene therapy of maturity onset diabetes in the young.Semantic proximity Read ↗

Diagnostic screening of MODY2/<i>GCK</i>mutations in the Norwegian MODY RegistrySemantic proximity Read ↗

Childhood-onset mild diabetes caused by a homozygous novel variant in the glucokinase gene.Semantic proximity Read ↗

Glucokinase gene mutation screening in Argentinean clinically characterized MODY patients.Semantic proximity Read ↗

Recognition and Management of Individuals With Hyperglycemia Because of a Heterozygous Glucokinase Mutation.Semantic proximity Read ↗

Identification of 14 new glucokinase mutations and description of the clinical profile of 42 MODY-2 families.Semantic proximity Read ↗

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