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Article

Mutations in KCNJ5 gene cause hyperaldosteronism.

Circulation research - 10 Jun 2011

Zennaro Maria-Christina, Jeunemaitre Xavier

Abstract excerpt

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Topics

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Share to Adenoma
Share to Aldosterone
Share to G Protein-Coupled Inwardly-Rectifying Potassium Channels
Share to KCNJ5 gene

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Share to Hypertension

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Source

Identifiers

PMID: 21659651
DOI: 10.1161/RES.0b013e318224a359

Genes

KCNJ5

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

Related research

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Research trail→

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Mutations in KCNJ5 gene cause hyperaldosteronism.PMID 21659651Read ↗

A novel somatic mutation 145-147delETEinsK in KCNJ5 increases aldosterone production.Semantic proximity Read ↗

Discordant Genotype-Phenotype Correlation in Familial Hyperaldosteronism Type III with KCNJ5 Gene Mutation: A Patient Report and Review of the LiteratureSemantic proximity Read ↗

A Novel Y152C KCNJ5 Mutation Responsible for Familial Hyperaldosteronism Type IIISemantic proximity Read ↗

[Research progress of KCNJ5 gene in aldosterone-producing adenoma].Semantic proximity Read ↗

A Novel Point Mutation in the KCNJ5 Gene Causing Primary Hyperaldosteronism and Early-Onset Autosomal Dominant HypertensionSemantic proximity Read ↗

How do Kir3.4 mutations cause hereditary hyperaldosteronism?Semantic proximity Read ↗

Primary aldosteronism and potassium channel mutations.Semantic proximity Read ↗

Role of KCNJ5 in familial and sporadic primary aldosteronism.Semantic proximity Read ↗

Familial hyperaldosteronism type III.Semantic proximity Read ↗

An Update on Familial Hyperaldosteronism.Semantic proximity Read ↗

KCNJ5 mutations in the National Institutes of Health cohort of patients with primary hyperaldosteronism: an infrequent genetic cause of Conn's syndrome.Semantic proximity Read ↗

An update on novel mechanisms of primary aldosteronismSemantic proximity Read ↗

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