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