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