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.