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