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Direct Synthesis of Lamin A, Bypassing Prelamin A Processing, Causes Misshapen Nuclei in Fibroblasts but No Detectable Pathology in Mice* - Journal of Biological Chemistry
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Familial lamin A/C mutation cardiomyopathy with arrhythmia substrate detected by cardiac magnetic resonance imaging and electroanatomical mapping - International Journal of Cardiology
Clinical and Functional Characterization of a Novel Mutation in Lamin A/C Gene in a Multigenerational Family with Arrhythmogenic Cardiac Laminopathy | PLOS ONE
Clinical and Functional Characterization of a Novel Mutation in Lamin A/C Gene in a Multigenerational Family with Arrhythmogenic Cardiac Laminopathy | PLOS ONE
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Autosomal dominant dilated cardiomyopathy with atrioventricular block: a lamin A/C defect-related disease - ScienceDirect
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Frontiers | Effect of Occurrence of Lamin A/C (LMNA) Genetic Variants in a Cohort of 101 Consecutive Apparent “Lone AF” Patients: Results and Insights
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Electropherogram of the lamin A/C gene. Electropherograms of control... | Download Scientific Diagram
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Lamin A/C mutation is independently associated with an increased risk of arterial and venous thromboembolic complications - International Journal of Cardiology
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Refractory ventricular arrhythmia in a patient with Lamin A/C (LMNA) cardiomyopathy successfully treated with thoracic bilateral stellate ganglionectomy - HeartRhythm Case Reports
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Role of nuclear Lamin A/C in cardiomyocyte functions - Carmosino - 2014 - Biology of the Cell - Wiley Online Library
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Phosphorylated Lamin A/C in the Nuclear Interior Binds Active Enhancers Associated with Abnormal Transcription in Progeria - ScienceDirect
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Lamin A/C haploinsufficiency causes dilated cardiomyopathy and apoptosis-triggered cardiac conduction system disease - Journal of Molecular and Cellular Cardiology
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