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Location of Mutation in the KCNQ1 and Phenotypic Presentation of Long QT Syndrome

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Year: 2003
Type: article
Study design: Observational Study
Source: Journal of Cardiovascular Electrophysiology
DOI: 10.1046/j.1540-8167.2003.03177.x
Authors: WOJCIECH ZAREBA, ARTHUR J. MOSS, GLORIA SHEU, ELIZABETH S. KAUFMAN, SILVIA PRIORI, G. MICHAEL VINCENT, JEFFREY A. TOWBIN, JESAIA BENHORIN, PETER J. SCHWARTZ, CARLO NAPOLITANO, W. JACKSON HALL, MARK T. KEATING, MING QI, JENNIFER L. ROBINSON, MARK L. ANDREWS
Institutions: University of Rochester Medicine, University of Rochester, MetroHealth, Case Western Reserve University, University of Pavia, Fondazione Salvatore Maugeri, University of Utah, Baylor College of Medicine, Bikur Cholim Hospital, Boston Children's Hospital
Language: English

Topic: Cardiac electrophysiology and arrhythmias
Subfield: Cardiology and Cardiovascular Medicine
Field: Medicine
Domain: Health Sciences
SDG: Good health and well-being

Open Access status: closed

Funder: National Heart, Lung, and Blood Institute
Awards: G1030097554, G183946747, LONG QT SYNDROME--GENETIC STUDIES, Long QT Syndrome: Population, Genetic & Cardiac Studies
OpenAlex ID: W1984486892
FWCI: 4.398
Cites: 24
Cited by: 75
Related to: 10
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