Homozygous NMNAT2 mutation in sisters with polyneuropathy and erythromelalgia (2019)

First Author: Huppke P
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