Aims Mutations in the lamin A/C gene (LMNA) cause a variety of clinical phenotypes,
including dilated cardiomyopathy. LMNA is one of the most prevalent mutated genes in …

Background: Mutation in the lamin A/C gene (LMNA) is associated with several cardiac
phenotypes, such as cardiac conduction disorders (CCD), atrial arrhythmia (AA), malignant …

Background—Mutations in LMNA (lamin A/C), which encodes lamin A and C, typically cause
age-dependent cardiac phenotypes, including dilated cardiomyopathy, cardiac conduction …

This study evaluated common clinical characteristics of patients with lamin A/C gene
mutations that cause either isolated dilated cardiomyopathy or dilated cardiomyopathy in …

Background: Mutations in LMNA are variably expressed and may cause cardiomyopathy,
atrioventricular block (AVB), or atrial arrhythmias (AAs) and ventricular arrhythmias (VA) …

Abstract Aims Lamin A/C (LMNA) mutations cause familial dilated cardiomyopathy (DCM)
with frequent conduction blocks and arrhythmias. We explored the prevalence, cardiac …

Introduction and objectives According to sudden cardiac death guidelines, an implantable
cardioverter-defibrillator (ICD) should be considered in patients with LMNA-related dilated …

Objectives: We examined the prevalence, genotype-phenotype correlation, and natural
history of lamin A/C gene (LMNA) mutations in subjects with dilated cardiomyopathy (DCM) …

Objective Mutations in the LMNA gene encoding lamins A and C of the nuclear lamina are a
frequent cause of cardiomyopathy accounting for 5–8% of familial dilated cardiomyopathy …

Objectives: The purpose of this study was to determine risk factors that predict malignant
ventricular arrhythmias (MVA) in Lamin A/C (LMNA) mutation carriers. Background: LMNA …