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Article

A novel nonsense mutation in GCK exon 9 co-segregates with diabetes phenotype.

Experimental and clinical endocrinology & diabetes : official journal, German Society of Endocrinology [and] German Diabetes Association - 1 Jun 2004

Knebel B, Jacob S, Boxberg C V, Müller-Wieland D, Kotzka J

Abstract excerpt

Maturity-onset diabetes of the young is an autosomal dominant form of non-insulin dependent diabetes mellitus and is caused by mutations in at least six different genes. In the most common forms, i.e. MODY2 and MODY3, the glucokinase (GCK) and the hepatocyte nuclear factor (HNF)-1alpha gene is af...

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Source

Identifiers

PMID: 15216446
DOI: 10.1055/s-2004-820967

Genes

GCK

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 1 Sept 2026. Prepared record publication-15216446-2026-09-01.1. Manifest publication-graph-cohort-2026-09-01.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 1 Sept 2026.

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