NMN Deamidase Delays Wallerian Degeneration and Rescues Axonal Defects Caused by NMNAT2 Deficiency In Vivo (2017)

First Author: Di Stefano M

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.9110

Publication URI: https://www.repository.cam.ac.uk/handle/1810/263744

Type: Journal Article/Review