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RNA interference AAV8 Dynamin 2 Caveolin-3 Atrial heart defects Satellite cell Gene therapy Becker muscular dystrophy BMD Autosomal dominant centronuclear myopathy Developmental biology Dynamine Cardiotoxin Clathrine Adult patients Cytosquelette Dynamin overexpression Muscle Adeno-associated virus Duchenne muscular dystrophy DMD Dynamin AFM Actin Cancer Outflow tract Cellules de crête neurale Amphiphysin Cytoskeleton BAR proteins Biomarkers Alpha-actinin-2 Caveolin Adeno-Associated virus Skeletal muscle CAV-3 gene AAV Caveolins Duchenne Muscular Dystrophy Core myopathy Congenital myopathy Nesprin Cell migration Autophagy Autophagosome maturation DNM2 Endocytosis Muscular dystrophy BAF Nuclear envelope Dominant centronuclear myopathy Cell signaling Dullard Adhesion Cardiomyopathies Ctdnep1 ACTN2 Cross-bridge kinetics Migration Disease modifiers Myosin Lamin BMP signaling Allele-specific silencing Domaine LEM Nucleus Coeur CAV3 Atrial cardiac defects Cellular neuroscience Antisense oligonucleotides Duchenne muscular dystrophy Autophagy cellular Adeno-associated virus vector Skin Charcot-Marie-Tooth Cavéoles Neural crest cells Animal models of human disease Biophysics Developmental myosin heavy chain Cavins Allele‐specific silencing therapy Diaphragm Autophagosome Cell proliferation CTL A-type lamins Allele specific RNA interference Mechanotransduction Correlative microscopy Myopathie Actin nucleus Myopathy Allele-specific silencing therapy AD-CNM DMyHC Disease heterogeneity Cross-presentation Clathrin Centronuclear myopathy Caveolae