CTG repeat contractions Congenital myopathy AAV Cytokines Animals Male Astrocyte Rare neuromuscular diseases Humans Autoantibodies Myotonic Dystrophy type 1 Heart Errance diagnostique Myasthenia Gravis MG Genotype phenotype correlation Fabry disease Myopathy Fibrosis Treatment Myotonic dystrophy type 1 Nuclear envelope Heart failure Neuromuscular diseases FSHD Myositis Neuromuscular junction Muscle regeneration Alternative splicing Lamin A/C LMNA gene Centronuclear myopathy LMNA COVID-19 Transcriptomics Myotonic Dystrophy Thérapie génique Myasthenia gravis Becker muscular dystrophy Myotonic dystrophy Dermatomyositis RNA interference Satellite cell Calcium Skeletal muscle Muscular dystrophy Cell therapy Congenital muscular dystrophy Motoneuron Neuromuscular disease Muscle MBNL Dynamin 2 Outcome measures Thymus Biomarkers Laminopathie Laminopathy Glutamate Lamin A/C Duchenne muscular dystrophy Cytoskeleton Autoimmunity Mice Myoblasts Dilated cardiomyopathy Therapy Biomarker Exercise Regeneration Mouse model Inflammation LMNA gene Myopathies Dystrophin Rare diseases Brain Satellite cells PABPN1 ALS Aged Laminopathies Spinal muscular atrophy Antisense oligonucleotides Long read sequencing Genetics CRISPRi Amyotrophic lateral sclerosis CMS Cardiomyopathy Autoimmune diseases Mechanotransduction Myogenesis DMD Gene therapy OPMD Transgenic mouse model Aging Actin Autophagy RNA biology Trinucleotide repeat expansion