Why the study?
Do different genetic loci for long QT syndrome (chromosomes 3, 7, 11) result in distinct phenotypic ECG T-wave patterns?
Population
153 members of six families with long QT syndrome linked to markers on chromosomes 3, 7, and 11
Comparison
Long QT syndrome genotypes vs Unaffected family members and cross-genotype…
Design
Cohort
Authors
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May aid LQTS genotype identification via ECG; extends correlations but leaves open impact on diagnosis or risk stratification.
Do different genetic loci for long QT syndrome (chromosomes 3, 7, 11) result in distinct phenotypic ECG T-wave patterns?
Moss et al. (1995) studied this question.
Synapse has enriched 3 closely related papers on similar clinical questions. Consider them for comparative context: