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/10.1016/j.cub.2017.01.070

PubMed Identifier: 28262487

Publication URI: http://europepmc.org/abstract/MED/28262487

Type: Journal Article/Review

Volume: 27

Parent Publication: Current biology : CB

Issue: 6

ISSN: 0960-9822