Dilated Cardiomyopathy: Genetic Determinants and Mechanisms
By E. McNally, L. Mestroni. Circulation Research, 2017
621 citations recorded by the source corpus.
Subfields: Cardiology and Cardiovascular Medicine
View Paper: https://www.semanticscholar.org/paper/8edafa411b5875ec01088f58c930010b6e819c79
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In Cardiology and Cardiovascular Medicine
Citations in the corpus
- 2019 HRS expert consensus statement on evaluation, risk stratification, and management of arrhythmogenic cardiomyopathy. (2019, background): “Specifically,MYH7 accounts for approximately 3%–4% of familial DCM cases.(339) Sarcomere gene variants contribute to cases of LVNC, althoughmost often in phenotypes that include another cardiomyopathy, cardiac malformation and/or reduced ejection fraction, with MYH7 variants contributing the most ca”