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