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LMNA gene COL6A3 Collagen VI-related myopathies NGS collagen type VI congenital muscular dystrophy CMD limb-girdle muscular dystrophy LGMD muscular MRI neuromuscular disorders Lamin A/C LMNA gene CMTX A-type lamins Myogenesis Emerin Acetyltransferase Angiotensin-converting enzyme inhibitors Alternative splicing Next generation sequencing LGMD Duchenne muscular dystrophy Biological sciences Clinical trial Muscle POPDC1 Rare neuromuscular diseases Mouse Rare diseases Butyrylcholinesterase C2C12 Neuromuscular diseases Adult SMA Mutations Exome Skeletal muscle LMNA Allele-specific silencing Lamin A/C nuclei Becker muscular dystrophy Treatment delay Cardiomyopathy Dynamin 2 Hypermobile EDS Myopathies Autophagosome maturation Myologie Nuclear envelope Gene Dilated cardiomyopathy Becker muscular dystrophy BMD Duchenne muscular dystrophy DMD miRNA nNOS INPP5K Muscular dystrophy MD Dystrophine Allele‐specific silencing therapy Angiotensin-converting enzyme inhibitor COVID-19 Lamin A/C Regeneration AAV Myopathy AAV VECTOR Centronuclear myopathy BVES CAV3 Gene therapy Titin LMNA-related congenital muscular dystrophy Laminopathie Laminopathies IPSC Actionability Errance diagnostique Biomarker Calcium handling Dystrophie musculaire GNE RNA interference Cancer biomarkers Muscle MRI Ehlers‐Danlos Syndrome Maladies rares Muscle biopsy COL6A1 Diagnosis Laminopathy CSF protein A-type lamin Actionable gene Patient registry BiP Cancer Base de données FAIR Connective tissue Congenital muscular dystrophy Maladies rares et orphelines Lamins Joint laxity Heart Myotubes Treatment COL1A1 C elegans Muscular dystrophy Therapy Heart failure CRISPR Emery-Dreifuss muscular dystrophy Allele-specific silencing therapy