Title: | The 2018 version of the gene table of monogenic neuromuscular disorders (nuclear genome) |
Journal : | Neuromuscular disorders : NMD, 27, 12 |
Authors: | Bonne G, Author ; Rivier F ; Hamroun D |
Material Type: | Article |
Publication Date: | 2017 |
Size: | p 1152 |
Languages: | English |
Keywords : | amyotrophic lateral sclerosis ; Charcot-Marie-Tooth disease ; chromosomes ; congenital muscular dystrophy ; congenital myasthenic syndrome ; congenital myopathy ; diseases classifications ; distal myopathy ; familial dilated cardiomyopathy ; familial hypertrophic cardiomyopathy ; genes ; genetic diseases ; hereditary metabolic myopathy ; inheritance ; ion channel disease ; malignant hyperthermia ; motor neuron disease ; muscular dystrophy ; myofibrillar myopathy ; myotonic syndrome ; neuromuscular disease ; nuclear genome ; progressive muscular dystrophy ; protein ; reference works ; spinal muscular atrophy |
Pubmed / DOI : | DOI : 10.1016/j.nmd.2017.10.005 / Pubmed : 29961566 |