Targeted therapies in genetic dilated and hypertrophic cardiomyopathies: from molecular mechanisms to therapeutic targets. A position paper from the Heart Failure Association (HFA) and the Working Group on Myocardial Function of the European Society of Cardiology (ESC)

Genetic cardiomyopathies are disorders of the cardiac muscle, most often explained by pathogenic mutations in genes encoding sarcomere, cytoskeleton, or ion channel proteins. Clinical phenotypes such as heart failure and arrhythmia are classically treated with generic drugs, but aetiology-specific a...

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Main Authors: Backs, J. (Author), Carrier, L. (Author), Coats, A.J.S (Author), de Boer, R.A (Author), Dimmeler, S. (Author), Eschenhagen, T. (Author), Filippatos, G. (Author), Gepstein, L. (Author), Heymans, S. (Author), Hulot, J.-S (Author), Knöll, R. (Author), Kupatt, C. (Author), Linke, W.A (Author), Seferovic, P.M (Author), Seidman, C.E (Author), Thum, T. (Author), Tocchetti, C.G (Author), van der Velden, J. (Author), Walsh, R. (Author)
Format: Article
Language:English
Published: John Wiley and Sons Ltd 2022
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