Variable clinical phenotype in TBK1 mutations: case report of a novel mutation causing primary progressive aphasia and review of the literature. (2021)
Attributed to:
The UK GENetic Frontotemporal dementia Initiative (UK GENFI)
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1016/j.neurobiolaging.2020.08.014
PubMed Identifier: 32980182
Publication URI: http://europepmc.org/abstract/MED/32980182
Type: Journal Article/Review
Volume: 99
Parent Publication: Neurobiology of aging
ISSN: 0197-4580