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Article

Lactose intolerance genetic testing: is it useful as routine screening? Results on 1426 south-central Italy patients.

Clinica chimica acta; international journal of clinical chemistry - 15 Jan 2015

Santonocito Concetta, Scapaticci Margherita, Guarino Donatella, Annicchiarico Eleonora Brigida, Lisci Rosalia, Penitente Romina, Gasbarrini Antonio, Zuppi Cecilia, Capoluongo Ettore

Abstract excerpt

Adult-type hypolactasia is a widespread condition throughout the world, causing lactose malabsorption. Several studies suggested that the identification of C/T-13910 and G/A-22018 mutations, located upstream the gene encoding the lactase-phlorizin hydrolase (LPH), is a useful tool for the differential diagnosis of hypolactasia. We evaluated the frequencies of C/T-13910 and G/A-22018 variants in a central-south...

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PMID: 25281930
DOI: 10.1016/j.cca.2014.09.026

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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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