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Variable clinical phenotype in TBK1 mutations: case report of a novel mutation causing primary progressive aphasia and review of the literature. (2021)

First Author: Swift IJ

Attributed to: Developing an evidence base for trials in genetic frontotemporal dementia - measures of disease onset and progression 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