Title: | The 2014 version of the gene table of monogenic neuromuscular disorders (nuclear genome) |
Journal : | Neuromuscular disorders : NMD, 23, 12 |
Authors: | Kaplan JC, Author ; Hamroun D |
Material Type: | Article |
Publication Date: | 2013 |
Size: | p 1081 |
Languages: | English |
Keywords : | Charcot-Marie-Tooth disease ; congenital muscular dystrophy ; congenital myasthenic syndrome ; congenital myopathy ; cross-sectional study ; diseases classifications ; familial dilated cardiomyopathy ; familial hypertrophic cardiomyopathy ; genes ; hereditary metabolic myopathy ; inheritance ; ion channel disease ; malignant hyperthermia ; motor neuron disease ; myofibrillar myopathy ; myotonic syndrome ; neuromuscular disease ; nuclear genome ; progressive muscular dystrophy ; protein ; reference works |
Pubmed / DOI : | DOI : 10.1016/j.nmd.2013.10.006 / Pubmed : 24446552 |