📣 Help Shape the Future of UKRI's Gateway to Research (GtR)

We're improving UKRI's Gateway to Research and are seeking your input! If you would be interested in being interviewed about the improvements we're making and to have your say about how we can make GtR more user-friendly, impactful, and effective for the Research and Innovation community, please email gateway@ukri.org.

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