Associated Papers
Advantages and Perils of Clinical Whole-Exome and Whole-Genome Sequencing in Cardiomyopathy.
Mazzarotto F et al.
Cardiovascular Drugs and Therapy, 2020
Digenic inheritance of mutations in the cardiac troponin (TNNT2) and cardiac beta myosin heavy chain (MYH7) as the cause of severe dilated cardiomyopathy.
Petropoulou E et al.
European Journal of Medical Genetics, 2017
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