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- W2469883669 abstract "Diseases related to lamin A/C mutations (laminopathies) are extremely heterogeneous. The common cardiac phenotype is idiopathic dilated cardiomyopathy with atrioventricular block and/or arrhythmias. Moreover, patients with lamin A/C gene mutations are at increased risk for sudden cardiac death. Here we present a family with a strong positive history of sudden cardiac death in presence of idiopathic dilated cardiomyopathy and cardiac conduction abnormalities, related to a novel lamin A/C mutation in exon 3." @default.
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- W2469883669 date "2010-03-01" @default.
- W2469883669 modified "2023-09-26" @default.
- W2469883669 title "[A novel lamin A/C mutation in a family with dilated cardiomyopathy and a strong history of sudden cardiac death]." @default.
- W2469883669 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/20461955" @default.
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