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