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Jonction neuro musculaire Acetyltransferase Alzheimer's disease Rare diseases CLS Embryo Aged Lithium chloride MBNL Deficiency IL-22 binding protein isoform Butyrylcholinesterase Brain Multiple sclerosis Precision medicine Treatment delay Epidemiology Mutation Knockout mouse Cell Cycle Proteins/chemistry/genetics/metabolism Heart failure Neuromuscular disease Body Patterning Gene Expression Regulation ALS HDAC motor neuron neuromuscular junction reinnervation Actin cytoskeleton Nondystrophic myotonias Longitudinal progression Adult SMA Gating pore current Abbreviations CMAP ¼ compound muscle action potential Animals Congenital myasthenic syndromes MRC ¼ Medical Research Council Experimental disease models Expression IL22RA2 Diseases Conduction disease Amyloid Acetylcholinesterase Distal myopathy Cytokines Paramyotonia congenita Synaptotagmin2 MuSK Cholinergic Cercopithecus aethiops Congenital myasthenic syndrome Clinical trials HEK293 Cells Neuromuscular junction Database Myotonia congenita Clinical trial Amyotrophic lateral sclerosis Aging Drainage Agrin Developmental Frontotemporal lobar degeneration Male Humans Awareness Motoneuron Chloride channel Dimerization M3243AG Autoimmune Acetylcholine receptor clustering Ca V COVID-19 NMJ Hypokalaemic periodic paralysis GFPT1 Female Genetic Association Studies Myotonic Dystrophy CMS Macrophages HypoPP ¼ hypokalaemic periodic paralysis Congenital myopathy MUNIX Calcium channel Receptors Minigene Cluster Analysis Actionable genes HSP70 Heat-Shock Proteins/genetics/metabolism Jonction Neuromusculaire NMJ Biological Markers Hereditary/genetics 80 and over Cognitive decline COS Cells Wnt Amyotrophic Lateral Sclerosis/genetics Chemokines Frontotemporal Dementia/genetics Jonction neuromusculaire LRP4