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