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