Matthew R G Taylor et al.
Journal of the American College of Cardiology, 41(5), 771-780 (2003-03-12)
We examined the prevalence, genotype-phenotype correlation, and natural history of lamin A/C gene (LMNA) mutations in subjects with dilated cardiomyopathy (DCM). Mutations in LMNA have been found in patients with DCM with familial conduction defects and muscular dystrophy, but the