Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Familial Hyperkalemic Hypertension Genotype With a Negative Phenotype: A CUL3 Mosaicism.

American journal of hypertension - 13 Mar 2020

Ostrosky-Frid Mauricio, Chávez-Canales María, Romo Miriam, Grunfeld Beatriz, Simsolo Rosa, Segura-Kato Yayoi, Tusié-Luna Teresa, Gamba Gerardo

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Blood Pressure
Share to Child
Share to Cullin Proteins
Share to Heredity

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Mosaicism

Share to Pedigree

Share to Pseudohypoaldosteronism

Share to Risk Factors

Source

Open in PubMed Open full text

Identifiers

PMID: 31802109
DOI: 10.1093/ajh/hpz185
PMCID: PMC13368862

Genes

CUL3

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Familial Hyperkalemic Hypertension Genotype With a Negative Phenotype: A CUL3 Mosaicism.PMID 31802109Read ↗

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

Hypertension: new roles for CUL-3 in the kidney.Semantic proximity Read ↗

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

[Channelopathies].Semantic proximity Read ↗

Potassium Channels: Molecular Defects, Diseases, and Therapeutic OpportunitiesSemantic proximity Read ↗

An update on novel mechanisms of primary aldosteronismSemantic proximity Read ↗

EAS Consensus Panel statement on homozygous FH.Semantic proximity Read ↗

Mutations in kelch-like 3 and cullin 3 cause hypertension and electrolyte abnormalities.Semantic proximity Read ↗

A CELSR1 variant in a patient with pulmonary arterial hypertension.Semantic proximity Read ↗

Functional studies of CYP21A2 mutants complement structural and clinical predictions of disease severity in CAH.Semantic proximity Read ↗

[SAC1 and SAC2: disease loci, gene defect, and clinical phenotypes].Semantic proximity Read ↗

Extending the clinical spectrum of SPG3A mutations to a very severe and very early complicated phenotype.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.