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