Integrated allelic, transcriptional, and phenomic dissection of the cardiac effects of titin truncations in health and disease

The recent discovery of heterozygous human mutations that truncate full-length titin (TTN, an abundant structural, sensory, and signaling filament in muscle) as a common cause of end-stage dilated cardiomyopathy (DCM) promises new prospects for improving heart failure management. However, realizatio... View More