Condition: Familial dilated cardiomyopathy


rs397517906 in LMNA gene and Familial dilated cardiomyopathy PMID 30402260 2018 Lamin mutation location predicts cardiac phenotype severity: combined analysis of the published literature.

PMID 30765282 2019 Heart failure in patients with arrhythmogenic right ventricular cardiomyopathy: Genetic characteristics.