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