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