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