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