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Article

Clinical and genetic investigation of pediatric cases of Wolff-Parkinson-White syndrome in Tunisian families.

Heart & lung : the journal of critical care - 1 Jan 2000

Nouira Sonia, Ouarda Fatma, Charfeddine Cherine, Arfa Imen, Ouragini Houyem, Abid Fekria, Abdelhak Sonia

Abstract excerpt

BACKGROUND: Wolff-Parkinson-White (WPW) syndrome is an autosomal-dominant heart disease characterized by an accessory pathway that arises from an aberrant conduction from the atria to the ventricles. Several mutations within the PRKAG2 gene were shown to be responsible for WPW. This gene encodes the γ2 regulatory subunit of adenosine monophosphate (AMP)-activated protein kinase, which functions as a metabolic...

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Source

Identifiers

PMID: 20561859
DOI: 10.1016/j.hrtlng.2009.10.012

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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