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