Striking phenotypic variation in a family with the P506S UBQLN2 mutation including amyotrophic lateral sclerosis, spastic paraplegia, and frontotemporal dementia. (2019)
Attributed to:
Exome sequencing in motor neuron disease: bioinformatic analyses and biological validation of novel variants
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
Volume: 73
Parent Publication: Neurobiology of aging
ISSN: 0197-4580