Title: | The 2016 version of the gene table of monogenic neuromuscular disorders (nuclear genome) |
Journal : | Neuromuscular disorders : NMD, 25, 12 |
Authors: | Kaplan JC, Author ; Hamroun D |
Material Type: | Article |
Publication Date: | 2015 |
Size: | p 991 |
Languages: | English |
Keywords : | Charcot-Marie-Tooth disease ; chromosomes ; congenital muscular dystrophy ; congenital myasthenic syndrome ; congenital myopathy ; cross-sectional study ; diseases classifications ; distal myopathy ; familial dilated cardiomyopathy ; familial hypertrophic cardiomyopathy ; genes ; hereditary metabolic myopathy ; inheritance ; ion channel disease ; late-onset Pompe disease ; malignant hyperthermia ; motor neuron disease ; myofibrillar myopathy ; myotonic syndrome ; neuromuscular disease ; nuclear genome ; progressive muscular dystrophy ; protein ; reference works |
Abstract: |
Corrigendum to “The 2016 version of the gene table of monogenic neuromuscular disorders (nuclear genome)” [Neuromuscular Disorders Volume 25 (2015) 991–1020]
ERRATUM: The authors and the editorial office regret the oversight of the journal reference under the title at the start of the Gene Table on page 993 which should read: Volume 25 No.12, December 2015. (Neuromuscul Disord. 2016 Apr-May;26(4-5):330. doi: 10.1016/j.nmd.2016.04.002. PMID: 27087612) |
Pubmed / DOI : | DOI : 10.1016/j.nmd.2015.10.010 / Pubmed : 27563712 |