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

A molecular basis for cardiac arrhythmia: HERG mutations cause long QT syndrome

1 Mar 1995

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 Cardiac electrophysiology and arrhythmias
Share to Cardiomyopathy and Myosin Studies
Share to Ion channel regulation and function

Source

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Identifiers

PMID: 7889573
DOI: 10.1016/0092-8674(95)90358-5

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

A molecular basis for cardiac arrhythmia: HERG mutations cause long QT syndromePMID 7889573Read ↗

Long QT syndrome: cellular basis and arrhythmia mechanism in LQT2.Semantic proximity Read ↗

hERG potassium channels and cardiac arrhythmia.Semantic proximity Read ↗

The long QT syndrome: a clinical counterpart of hERG mutations.Semantic proximity Read ↗

The long QT syndrome: ion channel diseases of the heart.Semantic proximity Read ↗

Long QT syndrome: novel insights into the mechanisms of cardiac arrhythmias.Semantic proximity Read ↗

Human ether-a-go-go related gene (hERG) K+ channels: function and dysfunction.Semantic proximity Read ↗

Congenital long QT syndromes: clinical features, molecular genetics and genetic testing.Semantic proximity Read ↗

Unraveling the genetics and mechanisms of cardiac arrhythmia.Semantic proximity Read ↗

Genetic basis of malignant channelopathies and ventricular fibrillation in the structurally normal heart.Semantic proximity Read ↗

Genetic and molecular basis of cardiac arrhythmias; impact on clinical management. Study group on molecular basis of arrhythmias of the working group on arrhythmias of the european society of cardiology.Semantic proximity Read ↗

The impact of recent advances in genetics in understanding disease mechanisms underlying the long QT syndromes.Semantic proximity Read ↗

Inherited arrhythmic disorders: long QT and Brugada syndromes.Semantic proximity Read ↗

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