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