The 2018 version of the gene table of monogenic neuromuscular disorders (nuclear genome) - Bonne, Gisèle; Rivier, François; Hamroun, Dalil (Neuromuscular disorders : NMD, 2017)
Keywords: Cell Nucleus - genetics; Chromosome Mapping; Cognitive science; Genetics; Genome - genetics; Human genetics; Humans; Life Sciences; Neuromuscular Diseases - genetics; Neuroscience; Ion channel muscle diseases; Congenital myasthenic syndromes; Congenital myopathies; Malignant hyperthermias; Motor neurone diseases; Myotonic syndromes; Hereditary cardiomyopathies; Hereditary ataxias; Other neuromuscular disorders; Hereditary motor and sensory neuropathies; Congenital muscular dystrophies; Metabolic myopathies; Muscular dystrophies; Hereditary paraplegias; Distal myopathies; Other myopathies