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Article

The Molecular Genetics of Gordon Syndrome.

Genes - 29 Nov 2019

Mabillard Holly, Sayer John A

Abstract excerpt

Gordon syndrome is a rare inherited monogenic form of hypertension, which is associated with hyperkalaemia and metabolic acidosis. Since the recognition of this predominantly autosomal dominant condition in the 1960s, the study of families with Gordon syndrome has revealed four genes WNK1, WNK4, KLHL3, and CUL3 to be implicated in its pathogenesis after a phenotype-genotype correlation was realised. The encoded...

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Identifiers

PMID: 31795491
DOI: 10.3390/genes10120986
PMCID: PMC6947027

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

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