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Article

A genetic test which can be used to diagnose adult-type hypolactasia in children.

Gut - 1 Nov 2004

Rasinperä H, Savilahti E, Enattah N S, Kuokkanen M, Tötterman N, Lindahl H, Järvelä I, Kolho K-L

Abstract excerpt

BACKGROUND/AIMS: Adult-type hypolactasia (primary lactose malabsorption) affects most of world's human population and limits the use of fresh milk due to lactose intolerance. The diagnosis of adult-type hypolactasia has been difficult to establish because of unsatisfactory diagnostic methods. C/T(-13910) single nucleotide polymorphism residing 13910 base pairs from the 5' end of the lactase gene has been shown to...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

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Identifiers

PMID: 15479673
DOI: 10.1136/gut.2004.040048
PMCID: PMC1774274

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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A genetic test which can be used to diagnose adult-type hypolactasia in children.PMID 15479673Read ↗

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Use of genetic testing for hypolactasia trait in the North Denmark Region.Semantic proximity Read ↗

The -13914G>A variant upstream of the lactase gene (LCT) is associated with lactase persistence/non-persistence.Semantic proximity Read ↗

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