Severe biallelic loss-of-function mutations in nicotinamide mononucleotide adenylyltransferase 2 (NMNAT2) in two fetuses with fetal akinesia deformation sequence. (2019)
Attributed to:
Variability in human axon survival
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1016/j.expneurol.2019.112961
PubMed Identifier: 31136762
Publication URI: http://europepmc.org/abstract/MED/31136762
Type: Journal Article/Review
Volume: 320
Parent Publication: Experimental neurology
ISSN: 0014-4886