Mutations in the Glycosyltransferase Domain of GLT8D1 Are Associated with Familial Amyotrophic Lateral Sclerosis. (2019)
Attributed to:
Exome sequencing in motor neuron disease: bioinformatic analyses and biological validation of novel variants
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1016/j.celrep.2019.02.006
PubMed Identifier: 30811981
Publication URI: http://europepmc.org/abstract/MED/30811981
Type: Journal Article/Review
Volume: 26
Parent Publication: Cell reports
Issue: 9