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