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