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