Lamin A/C Gene and the Heart
Author:
Publisher
Elsevier BV
Subject
Cardiology and Cardiovascular Medicine
Reference12 articles.
1. Human laminopathies: nuclei gone genetically awry;Capell;Nat Rev Genet,2006
2. The laminopathies: a clinical review;Rankin;Clin Genet,2006
3. Natural history of dilated cardiomyopathy due to lamin A/C gene mutations;Taylor;J Am Coll Cardiol,2003
4. Primary prevention of sudden death in patients with lamin A/C gene mutations;Meune;N Engl J Med,2006
5. Lamin A/C mutation analysis in a cohort of 324 unrelated patients with idiopathic or familial dilated cardiomyopathy;Parks;Am Heart J,2008
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1. LMNA Mutation in a Family with a Strong History of Sudden Cardiac Death;Genes;2022-01-19
2. Whole exome sequencing identified a pathogenic nonsense mutation in LMNA in a family with a progressive cardiac conduction defect: A case report;Molecular Medicine Reports;2020-04-01
3. Case reports of a c.475G>T, p.E159* lamin A/C mutation with a family history of conduction disorder, dilated cardiomyopathy and sudden cardiac death;BMC Cardiovascular Disorders;2019-12
4. Phenotypic and Genetic Characteristics of Lipodystrophy: Pathophysiology, Metabolic Abnormalities, and Comorbidities;Current Diabetes Reports;2018-11-08
5. Lamin mutation location predicts cardiac phenotype severity: combined analysis of the published literature;Open Heart;2018-10
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