Population
Transgenic mice with cardiac overexpression of mutant Desmoglein2 (Dsg2) Dsg2-N271S (Tg-NS/L)
Comparison
Cardiac overexpression of mutant Dsg2-N271S vs Mice with cardiac overexpression of wild-type…
Design
Preclinical
Authors
Loading...
Suggests early arrhythmogenic mechanisms in ARVC models; extends preclinical insights but leaves open human translation and therapeutic relevance.
In a mouse model of ARVC, mutant Dsg2 interacts with NaV1.5 and causes reduced Na+ current density and conduction slowing prior to overt structural cardiomyopathic changes.
Rizzo et al. (2012) studied this question.
Synapse has enriched 4 closely related papers on similar clinical questions. Consider them for comparative context: