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Article

Resistance to hypertension and high Cl- excretion in humans with SLC26A4 mutations.

Clinical genetics - 1 Mar 2017

Kim B G, Yoo T-H, Yoo J-E, Seo Y J, Jung J, Choi J Y

Abstract excerpt

Pendrin is a membrane transporter encoded by solute carrier family26A4 (SLC26A4). Mutations in this gene are known to cause hearing loss, and recent data from animal studies indicate a link between pendrin expression and hypertension; although, this association in humans is unclear. To clarify this issue, we investigated the influence of pendrin on blood pressure by analyzing demographic and biochemical data -...

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Identifiers

PMID: 27090054
DOI: 10.1111/cge.12789

Provenance

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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Resistance to hypertension and high Cl- excretion in humans with SLC26A4 mutations.PMID 27090054Read ↗

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