Myosin Clathrin Myopathie Duchenne Muscular Dystrophy Antisense oligonucleotides Actin Cytosquelette Animal models of human disease Core myopathy Neural crest cells Autosomal dominant centronuclear myopathy Satellite cell Dystrophin Outflow tract Allele-specific silencing therapy Congenital myopathy Nucleus CAV-3 gene AFM Cellules de crête neurale Clathrine Endocytosis Charcot-Marie-Tooth Skeletal muscle DNM2 Disease modifiers Cavéoles Atrial heart defects Cytoskeleton Cavins Developmental myosin heavy chain Dynamin 2 Domaine LEM Disease heterogeneity Autophagy Actin nucleus Lamin AAV Amphiphysin CTL Nuclear envelope Adult patients Centronuclear myopathy Allele specific RNA interference DMyHC Allele‐specific silencing therapy Dynamin ACTN2 Caveolins Cell migration Autophagosome maturation Adeno-Associated virus Cancer Alpha-actinin-2 Adeno-associated virus Cross-presentation Autophagosome Duchenne muscular dystrophy DMD BAF Mechanotransduction Diaphragm Cardiomyopathies Becker muscular dystrophy BMD AD-CNM Dullard Developmental biology Migration RNA interference Muscular dystrophy Adeno-associated virus vector Nesprin Dystrophie musculaire d'Emery Dreifuss Caveolin Cross-bridge kinetics Biophysics Duchenne muscular dystrophy Muscle Gene therapy Coeur Dynamine Atrial cardiac defects Biomarkers Cell signaling Dynamin overexpression Dystrophie musculaire de Duchenne A-type lamins Dominant centronuclear myopathy Cellular neuroscience Allele-specific silencing BAR proteins AAV8 Cardiotoxin BMP signaling Caveolae Skin Myopathy Cell proliferation Correlative microscopy Adhesion Ctdnep1