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