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