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

Molecular genetic analysis of PRKAG2 in sporadic Wolff-Parkinson-White syndrome.

Journal of cardiovascular electrophysiology - 1 Mar 2003

Vaughan Carl J, Hom Yolanda, Okin Daniel A, McDermott Deborah A, Lerman Bruce B, Basson Craig T

Abstract excerpt

INTRODUCTION: Mutations in the PRKAG2 gene that encodes the gamma2 regulatory subunit of AMP-activated protein kinase have been shown to cause autosomal dominant Wolff-Parkinson-White (WPW) syndrome associated with hypertrophic cardiomyopathy. Prior studies focused on familial WPW syndrome associated with other heart disease such as hypertrophic cardiomyopathy. However, such disease accounts for only a small...

Read the complete abstract on PubMed

Topics

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

Share to Adolescent
Share to Aged, 80 and over

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to AMP-Activated Protein Kinases

Share to Catheter Ablation

Share to Introns

Share to Multienzyme Complexes

Share to Polymorphism, Genetic

Share to Protein Serine-Threonine Kinases

Source

Identifiers

PMID: 12716108
DOI: 10.1046/j.1540-8167.2003.02394.x

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.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Molecular genetic analysis of PRKAG2 in sporadic Wolff-Parkinson-White syndrome.PMID 12716108Read ↗

Familial Pseudo‐Wolff‐Parkinson‐White SyndromeSemantic proximity Read ↗

Identification of a Gene Responsible for Familial Wolff–Parkinson–White SyndromeSemantic proximity Read ↗

PRKAG3 polymorphisms associated with sporadic Wolff-Parkinson-White syndrome among a Taiwanese population.Semantic proximity Read ↗

Wolff-Parkinson-White syndrome: De novo variants and evidence for mutational burden in genes associated with atrial fibrillation.Semantic proximity Read ↗

PRKAG2 mutation: An easily missed cardiac specific non-lysosomal glycogenosisSemantic proximity Read ↗

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

Mutation analysis of AMP-activated protein kinase subunits in inherited cardiomyopathies: implications for kinase function and disease pathogenesis.Semantic proximity Read ↗

Transgenic mice overexpressing mutant PRKAG2 define the cause of Wolff-Parkinson-White syndrome in glycogen storage cardiomyopathy.Semantic proximity Read ↗

Cardiac manifestations of PRKAG2 mutation.Semantic proximity Read ↗

Familial Wolff-Parkinson-White Syndrome: a disease of glycogen storage or ion channel dysfunction?Semantic proximity Read ↗

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

Novel PRKAG2 mutation responsible for the genetic syndrome of ventricular preexcitation and conduction system disease with childhood onset and absence of cardiac hypertrophy.Semantic proximity Read ↗

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