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Two pathologically confirmed cases of novel mutations in the MAPT gene causing frontotemporal dementia. (2020)

First Author: Shafei R

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.2019.11.009

PubMed Identifier: 31870644

Publication URI: http://europepmc.org/abstract/MED/31870644

Type: Journal Article/Review

Volume: 87

Parent Publication: Neurobiology of aging

ISSN: 0197-4580