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A recessive S174X mutation in Optineurin causes amyotrophic lateral sclerosis through a loss of function via allele-specific nonsense-mediated decay. (2021)

First Author: Gotkine M

Attributed to: Capital award for UK DRI at King's College London funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1016/j.neurobiolaging.2021.05.009

PubMed Identifier: 34272080

Publication URI: http://europepmc.org/abstract/MED/34272080

Type: Journal Article/Review

Volume: 106

Parent Publication: Neurobiology of aging

ISSN: 0197-4580