Associated Papers
The penetrance of rare variants in cardiomyopathy-associated genes: A cross-sectional approach to estimating penetrance for secondary findings.
McGurk KA et al.
American Journal of Human Genetics, 2023
37652022 (PubMed )
Supplement: mmc3.xlsx › Table_S9
Functional Epicardial Conduction Disturbances Due to a SCN5A Variant Associated With Brugada Syndrome.
Renard E et al.
Jacc. Clinical Electrophysiology, 2023
37227351 (PubMed )
Supplement: mmc1.docx
Reevaluating the Genetic Contribution of Monogenic Dilated Cardiomyopathy.
Mazzarotto F et al.
Circulation, 2020
31983221 (PubMed )
Supplement: cir-141-387-s002.xlsx › Table_S3
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