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