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Genes | Free Full-Text | Splicing Variants, Protein-Protein Interactions, and Drug Targeting in Hutchinson-Gilford Progeria Syndrome and Small Cell Lung Cancer
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The role of genetic mutations in genes LMNA, PPARG, PLIN1, AKT2, CIDEC in Köbberling–Dunnigan Syndrome
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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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Modulation of cytoskeleton in cardiomyopathy caused by mutations in LMNA gene | American Journal of Physiology-Cell Physiology
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LMNA mutations detected in patients. (A) Representation of mutations... | Download Scientific Diagram
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Increased expression of the Hutchinson–Gilford progeria syndrome truncated lamin A transcript during cell aging | European Journal of Human Genetics
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Pathogenic LMNA variants disrupt cardiac lamina-chromatin interactions and de-repress alternative fate genes - ScienceDirect
Whole-Exome Sequencing to Identify a Novel LMNA Gene Mutation Associated with Inherited Cardiac Conduction Disease | PLOS ONE
David R. Liu on X: "The mutation (discovered by @NIHDirector's lab in 2003) results in progerin, a toxic protein that damages nuclei. So providing more healthy LMNA is not a solution, and
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Generation of Lamin A/C gene (Lmna) exon 4 mutations using CRISPR/Cas... | Download Scientific Diagram
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