Identification of a Gene Responsible for Familial Wolff–Parkinson–White Syndrome
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Open Access
- 14 June 2001
- journal article
- research article
- Published by Massachusetts Medical Society in New England Journal of Medicine
- Vol. 344 (24) , 1823-1831
- https://doi.org/10.1056/nejm200106143442403
Abstract
The Wolff–Parkinson–White syndrome, with a prevalence in Western countries of 1.5 to 3.1 per 1000 persons, causes considerable morbidity and may cause sudden death. We identified two families in which the Wolff–Parkinson–White syndrome segregated as an autosomal dominant disorder.Keywords
This publication has 20 references indexed in Scilit:
- Characterization of AMP-activated protein kinase γ-subunit isoforms and their role in AMP bindingBiochemical Journal, 2000
- The activation of p38 MAPK by the β‐adrenergic agonist isoproterenol in rat epididymal fat cellsFEBS Letters, 1998
- Familial Hypertrophic cardiomyopathy with Wolff-Parkinson-White syndrome maps to a locus on chromosome 7q3.Journal of Clinical Investigation, 1995
- Young adult survivors of sudden cardiac arrest: Analysis of invasive evaluation of 22 subjectsAmerican Heart Journal, 1989
- “Nodoventricular” accessory pathway: Evidence for a distinct accessory atrioventricular pathway with atrioventricular node-like propertiesJournal of the American College of Cardiology, 1988
- Cardiac arrest in young, ostensibly healthy patients: Clinical, hemodynamic, and electrophysiologic findingsThe American Journal of Cardiology, 1983
- Paroxysmal atrial fibrillation in the wolff-parkinson-white syndromeThe American Journal of Cardiology, 1981
- Atrial fibrillation in the preexcitation syndromeThe American Journal of Cardiology, 1977
- The electrocardiographic syndrome of short P-R interval and broad QRS complexes: A clinical study of 80 casesAmerican Heart Journal, 1957
- Analysis of the Electrocardiograms Obtained from 1000 Young Healthy AviatorsCirculation, 1954