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Article

D28G mutation in congenital glucose-galactose malabsorption.

Archives of Iranian medicine - 1 Oct 2007

Kianifar Hamid-Reza, Talebi Saeed, Talebi Saeed, Tavakkol-Afshari Jalil, Esmaili Mohammad, Davachi Behrouz, Brook Azam

Abstract excerpt

BACKGROUND: Congenital glucose-galactose malabsorption is a rare autosomal recessive disorder of the intestinal transport of glucose and galactose, leading to watery diarrhea, dehydration, failure to thrive, and early death. METHODS: In this study, we analyzed D28G mutation in 16 family members of a patient with typical presentation of congenital glucose-galactose malabsorption with polymerase chain...

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PMID: 17903058

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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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