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A case of lamin A/C mutation cardiomyopathy with overlap features of ARVC: A critical role of genetic testing - International Journal of Cardiology
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A progeria mutation reveals functions for lamin A in nuclear assembly, architecture, and chromosome organization | PNAS
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p.S143P mutant lamin A/C is more nucleoplasmic than WT lamin A/C and... | Download Scientific Diagram
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Generation of Lamin A/C gene (Lmna) exon 4 mutations using CRISPR/Cas... | Download Scientific Diagram
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The Cardiomyopathy Lamin A/C D192G Mutation Disrupts Whole-Cell Biomechanics in Cardiomyocytes as Measured by Atomic Force Microscopy Loading-Unloading Curve Analysis | Scientific Reports
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Frontiers | The Broad Spectrum of LMNA Cardiac Diseases: From Molecular Mechanisms to Clinical Phenotype
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Tyrosine phosphorylation of lamin A by Src promotes disassembly of nuclear lamina in interphase | Life Science Alliance
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The K219T-Lamin mutation induces conduction defects through epigenetic inhibition of SCN5A in human cardiac laminopathy | Nature Communications
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Missense Mutations in the Rod Domain of the Lamin A/C Gene as Causes of Dilated Cardiomyopathy and Conduction-System Disease | NEJM
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Lamin A/C protein (top), gene structure (middle), and localization of... | Download Scientific Diagram
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Dual Specificity Phosphatase 4 Mediates Cardiomyopathy Caused by Lamin A/C (LMNA) Gene Mutation* - Journal of Biological Chemistry
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