Minor hypertrophic cardiomyopathy genes, major insights into the genetics of cardiomyopathies
Hypertrophic cardiomyopathy (HCM) was traditionally described as an autosomal dominant
Mendelian disease but is now increasingly recognized as having a complex genetic …
Mendelian disease but is now increasingly recognized as having a complex genetic …
De novo and inherited variants in coding and regulatory regions in genetic cardiomyopathies
Background Cardiomyopathies are a leading cause of progressive heart failure and sudden
cardiac death; however, their genetic aetiology remains poorly understood. We …
cardiac death; however, their genetic aetiology remains poorly understood. We …