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/10.1101/610907
Publication URI: http://dx.doi.org/10.1101/610907
Type: Preprint