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Therapy Laminopathie AAV VECTOR C2C12 Acetyltransferase CRISPR LMNA gene Maladies rares et orphelines Angiotensin-converting enzyme inhibitor A-type lamins Base de données FAIR Exome Heart failure Angiotensin-converting enzyme inhibitors Next generation sequencing Myopathy Emery-Dreifuss muscular dystrophy Connective tissue Gene therapy LGMD Maladies rares Regeneration Dystrophine Muscle biopsy Dilated cardiomyopathy Treatment delay LMNA-related congenital muscular dystrophy Myologie Actionable gene Lamin A/C Dynamin 2 Myogenesis Cardiomyopathy Adult SMA Muscular dystrophy MD Errance diagnostique Biological sciences Becker muscular dystrophy BMD Duchenne muscular dystrophy DMD miRNA nNOS Heart Cardiac conduction system C elegans IPSC Neuromuscular diseases Duchenne muscular dystrophy Ehlers‐Danlos Syndrome Hypermobile EDS Allele-specific silencing Allele-specific silencing therapy Myotubes Butyrylcholinesterase BiP COL1A1 Mutations Skeletal muscle Congenital muscular dystrophy Emerin A-type lamin CMTX AAV Nuclear envelope Muscular dystrophy Myopathies Cancer LMNA Joint laxity Titin Lamin A/C nuclei Treatment RNA interference Actionability Diagnosis Muscle Calcium handling GNE COL6A1 Lamin A/C LMNA gene Laminopathy Laminopathies Cardiology Becker muscular dystrophy Cancer biomarkers Muscle MRI BVES Lamins Autophagosome maturation Allele‐specific silencing therapy Rare diseases Clinical trial INPP5K Centronuclear myopathy COVID-19 Dystrophie musculaire Biomarker POPDC1 Alternative splicing Mouse Patient registry CSF protein COL6A3 Collagen VI-related myopathies NGS collagen type VI congenital muscular dystrophy CMD limb-girdle muscular dystrophy LGMD muscular MRI neuromuscular disorders Rare neuromuscular diseases