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

First Author: Huppke P
Attributed to:  Variability in human axon survival funded by MRC


No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1016/j.expneurol.2019.112958

PubMed Identifier: 31132363

Publication URI: http://europepmc.org/abstract/MED/31132363

Type: Journal Article/Review

Volume: 320

Parent Publication: Experimental neurology

ISSN: 0014-4886