Homozygous mutation in the Neurofascin gene affecting the glial isoform of Neurofascin causes severe neurodevelopment disorder with hypotonia, amimia and areflexia. (2018)
Attributed to:
Imaging the assembly, disruption and restoration of nodes of Ranvier in myelinated nerves
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1093/hmg/ddy277
PubMed Identifier: 30124836
Publication URI: http://europepmc.org/abstract/MED/30124836
Type: Journal Article/Review
Volume: 27
Parent Publication: Human molecular genetics
Issue: 21
ISSN: 0964-6906