Mutations in PDLIM5 are rare in dilated cardiomyopathy but are emerging as potential disease modifiers.

<h4>Background</h4>A causal genetic mutation is found in 40% of families with dilated cardiomyopathy (DCM), leaving a large percentage of families genetically unsolved. This prevents adequate counseling and clear recommendations in these families. We aim to identify novel genes or modifiers associat... View More