The 2018 version of the gene table of monogenic neuromuscular disorders (nuclear genome)

Saved in:

Bibliographic Details
Published in	Neuromuscular disorders : NMD Vol. 27; no. 12; pp. 1152 - 1183
Main Authors	Bonne, Gisèle, Rivier, François, Hamroun, Dalil
Format	Journal Article
Language	English
Published	England Elsevier B.V 01.12.2017 Elsevier
Subjects	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
Online Access	Get full text
ISSN	0960-8966 1873-2364 1873-2364
DOI	10.1016/j.nmd.2017.10.005

More Information
Bibliography:	ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23
ISSN:	0960-8966 1873-2364 1873-2364
DOI:	10.1016/j.nmd.2017.10.005