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A novel LMNA mutation identified in a Japanese patient with LMNA-associated congenital muscular dystrophy | Human Genome Variation
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Clinical trial in a dish using iPSCs shows lovastatin improves endothelial dysfunction and cellular cross-talk in LMNA cardiomyopathy
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JCI - Activation of MAPK pathways links LMNA mutations to cardiomyopathy in Emery-Dreifuss muscular dystrophy
Whole-Exome Sequencing to Identify a Novel LMNA Gene Mutation Associated with Inherited Cardiac Conduction Disease | PLOS ONE
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r - ANOVA "Error in lm.fit(x, y, offset = offset, singular.ok = singular.ok, ...) : 0 (non-NA) cases" - Stack Overflow
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LMNA mutations detected in patients. (A) Representation of mutations... | Download Scientific Diagram
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Frontiers | The Emerging Role of Lamin C as an Important LMNA Isoform in Mechanophenotype | Cell and Developmental Biology
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Integrated analysis reveals the alterations that LMNA interacts with euchromatin in LMNA mutation-associated dilated cardiomyopathy | Clinical Epigenetics | Full Text
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Pathogenic LMNA variants disrupt cardiac lamina-chromatin interactions and de-repress alternative fate genes - ScienceDirect
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