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