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