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Article

Assessment of the CFTR and ENaC association.

Molecular bioSystems - 1 Feb 2009

Berdiev Bakhrom K, Qadri Yawar J, Benos Dale J

Abstract excerpt

Cystic fibrosis (CF) is one of the most common lethal genetic disorders. It results primarily from mutations in the cystic fibrosis transmembrane conductance regulator (cftr) gene. These mutations cause inadequate functioning of CFTR, which in turn leads to the severe disruption of transport function in several epithelia across various organs. Affected organs include the sweat glands, the intestine, and the...

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Source

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Identifiers

PMID: 19156256
DOI: 10.1039/b810471a
PMCID: PMC2666849

Genes

CFTR

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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