A nonsense mutation in myelin protein zero causes congenital hypomyelination neuropathy through altered P0 membrane targeting and gain of abnormal function. (2019)
Attributed to:
Investigating deficits of axonal RNA metabolism and axonal signalling in amyotrophic lateral sclerosis
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1093/hmg/ddy336
PubMed Identifier: 30239779
Publication URI: http://europepmc.org/abstract/MED/30239779
Type: Journal Article/Review
Volume: 28
Parent Publication: Human molecular genetics
Issue: 1
ISSN: 0964-6906