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Article

Familial hyperkalemic hypertension: phenotypic analysis in a large family with the WNK1 deletion mutation.

The American journal of medicine - 15 Apr 2003

Achard Jean-Michel, Warnock David G, Disse-Nicodème Sandra, Fiquet-Kempf Béatrice, Corvol Pierre, Fournier Albert, Jeunemaitre Xavier

Abstract excerpt

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Topics

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Share to Hyperkalemia
Share to Hypertension
Share to Intracellular Signaling Peptides and Proteins

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Introns

Share to Minor Histocompatibility Antigens

Share to Pseudohypoaldosteronism

Share to Syndrome

Share to WNK Lysine-Deficient Protein Kinase 1

Source

Identifiers

PMID: 12727582
DOI: 10.1016/s0002-9343(03)00054-8

Genes

WNK1

Provenance

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

Related research

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Click a neighbor to travelStep 1 · 12 closest

Familial hyperkalemic hypertension: phenotypic analysis in a large family with the WNK1 deletion mutation.PMID 12727582Read ↗

Human hypertension caused by mutations in WNK kinases.Semantic proximity Read ↗

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Familial Hyperkalemic Hypertension Genotype With a Negative Phenotype: A CUL3 Mosaicism.Semantic proximity Read ↗

The variety of genetic defects explains the phenotypic heterogeneity of Familial Hyperkalemic HypertensionSemantic proximity Read ↗

Mutation affecting the conserved acidic WNK1 motif causes inherited hyperkalemic hyperchloremic acidosis.Semantic proximity Read ↗

Hypercalciuria in familial hyperkalemia and hypertension accompanies hyperkalemia and precedes hypertension: description of a large family with the Q565E WNK4 mutation.Semantic proximity Read ↗

Wnk1 kinase deficiency lowers blood pressure in mice: a gene-trap screen to identify potential targets for therapeutic intervention.Semantic proximity Read ↗

WNK kinases and essential hypertension.Semantic proximity Read ↗

Deletion of WNK1 First Intron Results in Misregulation of Both Isoforms in Renal and Extrarenal TissuesSemantic proximity Read ↗

Pathogenesis of pseudohypoaldosteronism type 2 by WNK1 mutations.Semantic proximity Read ↗

WNK Kinases, Renal Ion Transport and HypertensionSemantic proximity Read ↗

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