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