Homozygous NMNAT2 mutation in sisters with polyneuropathy and erythromelalgia. (2019)
Attributed to:
Variability in human axon survival
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.17863/cam.40131
Publication URI: https://www.repository.cam.ac.uk/handle/1810/292980
Type: Journal Article/Review