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