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Isolated homozygous R217X OPTN mutation causes knock-out of functional C-terminal optineurin domains and associated oligodendrogliopathy-dominant ALS-TDP. (2021)

First Author: Nolan M

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