Isolated homozygous R217X OPTN mutation causes knock-out of functional C-terminal optineurin domains and associated oligodendrogliopathy-dominant ALS-TDP. (2021)
Attributed to:
MRC Brain Banks: Joint Application to Underpin Neuroscience Research
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1136/jnnp-2020-325803
PubMed Identifier: 33727253
Publication URI: http://europepmc.org/abstract/MED/33727253
Type: Journal Article/Review
Volume: 92
Parent Publication: Journal of neurology, neurosurgery, and psychiatry
Issue: 9
ISSN: 0022-3050