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