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