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Striking phenotypic variation in a family with the P506S UBQLN2 mutation including amyotrophic lateral sclerosis, spastic paraplegia, and frontotemporal dementia (2019)

First Author: Gkazi S

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.2018.08.015

PubMed Identifier: 30348461

Publication URI: http://europepmc.org/abstract/MED/30348461

Type: Journal Article/Review

Parent Publication: Neurobiology of Aging

ISSN: 0197-4580