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Centronuclear myopathy Gene editing PCR Genotype phenotype correlation Muscular dystrophy Hypoxia Aging Acetylcholinesterase knockout mouse Duchenne muscular dystrophy Glucocorticoid-receptor Muscle GABA Dilated cardiomyopathy CTG repeat contractions Diaphragm Alternative splicing Astrocytes Antisense oligonucleotides Myotonic dystrophy mouse models Intermediate filament ACETYLCHOLINESTERASE Autophagy Cells Dystrophin Animals Trinucleotide Repeat Expansion Thérapie génique Myelin CRISPR/Cas9 Brain Long read sequencing PacBio Acute coronary syndrome Glutamate Myostatin MBNL Glial cells Cultured Heart Dystrophie Myotonique AAV Maximal force Skeletal muscle Dystrophie myotonique Therapy Gene Therapy DMSXL mice Myotonic Dystrophy Glucocorticoids Humans RNA splicing Transcriptomics Dynamin 2 Expression Myotonic Dystrophy Type 1 CONGENITAL MYATHENIC SYNDROME Desmin DM1 Cardiac muscle CTG repeats Oligodendrocytes Trinucleotide repeat expansion Brain dysfunction Transgenic mouse model Cell culture model Myotonic dystrophy Cell penetrating peptide Exercise Male Cell model KNOCKOUT MICE Neuron Mouse models Acetylcholinesterase deficiency ARN Myotonic Dystrophy type 1 Endurance training Exercice BIOLOGIE MOLECULAIRE Motoneuron Gene therapy Astrocyte CMS CTG repeat instability Myotonic dystrophy type 1 Mice Oligodendrocyte Heart failure RNA interference DMPK Cytoskeleton Fibrosis Antisense oligonucleotide Central nervous system CRISPRi Quantitative microdialysis GSK3␤ Transgenic mouse RNA biology Mouse model