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A novel mutation of the LMNA gene in a family with dilated cardiomyopathy, conduction system disease, and sudden cardiac death of young females.
Identification of novel mutations in LMNA associated with familial forms of dilated cardiomyopathy.
Lamin A/C mutations associated with familial and sporadic cases of dilated cardiomyopathy in Koreans.
Electrophysiological and histopathological characteristics of progressive atrioventricular block accompanied by familial dilated cardiomyopathy caused by a novel mutation of lamin A/C gene.
Familial dilated cardiomyopathy and isolated left ventricular noncompaction associated with lamin A/C gene mutations.