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Article

The DG10S478 variant in the TCF7L2 gene is not associated with microvascular complications in type 2 diabetes.

Experimental and clinical endocrinology & diabetes : official journal, German Society of Endocrinology [and] German Diabetes Association - 1 Apr 2008

Buchbinder S, Rudofsky G, Humpert P M, Schilling T, Zorn M, Bierhaus A, Nawroth P P

Abstract excerpt

OBJECTIVE: The DG10S478 variant in the transcription factor 7-like 2 (TCF7L2) gene is a tetranucleotide repeat with six alleles. Alleles 0, 8 and 12 were found to account for 98% of chromosomes in population based controls. The composite allele X (non zero) has been associated with type 2 diabete...

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Source

Identifiers

PMID: 18072015
DOI: 10.1055/s-2007-993149

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-18072015-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

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

Related research

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The DG10S478 variant in the TCF7L2 gene is not associated with microvascular complications in type 2 diabetes.PMID 18072015Read ↗

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