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

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

Volume: 73

Parent Publication: Neurobiology of aging

ISSN: 0197-4580