Introduction: Gap junction channels are important determinants of conduction in the heart and may play a central role in the development of lethal cardiac arrhythmias, The recent development of a Cx43-deficient mouse has raised fundamental questions about the role of specific connexin isoforms in intercellular communication in the heart. Although a homozygous null mutation of the Cx43 gene (Cx43(-/-)) is lethal, the heterozygous (Cx43(+/-)) animals survive to adulthood. Reports on the cardiac electrophysiologic phenotype of the Cx43(+/-) mice are contradictory. Thus, the effects of a null mutation of a single Cx43 allele require reevaluation. Methods and Results: High-resolution video mapping techniques were used to study propagation in hearts from Cx43(+/-) and littermate control (Cx43(+/+)) mice. Local conduction velocities (CVs) and conduction patterns were quantitatively measured by determining conduction vectors. We undertook the characterization of ECG parameters and epicardial CVs of normal and Cx43(+/-) mouse hearts. ECG measurements obtained from 12 Cx43(+/+) and 6 Cx43(+/-) age matched mice did not show differences in any parameter, including QRS duration (14.5 +/- 0.9 and 15.7 +/- 2.3 msec for Cx43(+/+) and Cx43(+/-), respectively), In addition, using a sensitive method of detecting changes in local CV, video images of epicardial wave propagation revealed similar activation patterns and velocities in both groups of mice. Conclusion: A sensitive method that accurately measures local CVs throughout the ventricles revealed no changes in Cx43(+/-) mice, which is consistent with the demonstration that ECG parameter values in the heterozygous mice are the same as those in wild-type mice.