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Cardiomyopathies Agrin H-Adrenergic Cardiomyopathie Distal myopathy Dilated cardiomyopathy Muscular dystrophy Genetic background High-throughput screening Death Fibrin Drug repurposing ALS HDAC motor neuron neuromuscular junction reinnervation Dystrophin Ca 2+ sensitivity Emery-Dreifuss muscular dystrophy DMD Cardiology Chromosome 1q CLS Cardiomyopathy ALS amyotrophic lateral sclerosis Deficiency Emery-Dreifuss Muscular Dystrophy type 2 EDMD2 Anthropology Bioengineering CyTOF Covid 19 Actin Cardiac conduction system Genetics research LMNA Hutchinson-Gilford progeria syndrome Development Cellules musculaires lisses vasculaires Cardiovascular disease Lamin Emery-Dreifuss muscular dystrophy EDMD Autophagy/lysosomal pathway Connexin Butyrylcholinesterase Guyane Francaise Biomatériaux Ethnobotany Dental infection HBV Nuclear envelope Frank-Starling law France Hésitation vaccinale Anthropologie Animal model Electrocardiography Calcium Channelopathies Congenital myasthenic syndrome French Guiana C9ORF72 LMNA gene HIV Expression Energy metabolism Domestic Satellite cells Canine Epidemiology A-type lamins Apoptosis Microtubules Skeletal muscle Antilles Françaises Calcium handling Cellules souches Physiopathologic mechanism muscular dystrophy Dilated Cardiomyopathy CMD1A Fusion Emery–Dreifuss muscular dystrophy Cellules satellite French West Indies Dp71 Acetyltransferase Epizootic Muscle regeneration Sarcolipin CMS Biophysique Electrophysiology Ethnobotanique Genome organization Cofilin-1 Emerin Dog Defibrillators Progeria Aging Confinement Bioingénierie ERK1/2 signaling FTD frontotemporal dementia Neuromuscular disease