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Article

PRKAG2 cardiac syndrome: familial ventricular preexcitation, conduction system disease, and cardiac hypertrophy.

Current opinion in cardiology - 1 May 2002

Gollob Michael H, Green Martin S, Tang Anthony S L, Roberts Robert

Abstract excerpt

Genetic studies of families with inherited cardiac rhythm disturbances have established a molecular basis for ventricular arrhythmogenic disorders. Genes responsible for the long QT syndrome, Brugada syndrome, and polymorphic ventricular tachycardia have been identified. The elucidation of genetic defects responsible for more commonly occurring supraventricular rhythm disturbances have not been as forthcoming,...

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Source

Identifiers

PMID: 12015471
DOI: 10.1097/00001573-200205000-00004

Genes

PRKAG2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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PRKAG2 cardiac syndrome: familial ventricular preexcitation, conduction system disease, and cardiac hypertrophy.PMID 12015471Read ↗

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Identification of a novel de novo mutation associated with PRKAG2 cardiac syndrome and early onset of heart failure.Semantic proximity Read ↗

Ventricular pre-excitation and cardiac hypertrophy mimicking hypertrophic cardiomyopathy in a Turkish family with a novel PRKAG2 mutation.Semantic proximity Read ↗

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