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Article

Genetic Disorders of Membrane Transport III. Congenital chloride diarrhea.

The American journal of physiology - 1 Jan 1999

Kere J, Lohi H, Höglund P

Abstract excerpt

Congenital chloride diarrhea (CLD) is a recessively inherited disorder of intestinal electrolyte absorption that involves, specifically, Cl-/HCO-3 exchange. CLD is caused by mutations in a chromosome 7 gene, first known as DRA (for downregulated in adenoma). The disease occurs in all parts of the...

Topics

Bacterial Proteins
Chlorides
Diarrhea
Humans
Intestinal Mucosa
Models, Genetic
Mutation

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 9886972
DOI: 10.1152/ajpgi.1999.276.1.G7

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 30 Aug 2026. Prepared record publication-9886972-2026-08-30.1. Manifest publication-graph-cohort-2026-08-30.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 30 Aug 2026.

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