Potential genetic modifiers of disease risk and age at onset in patients with frontotemporal lobar degeneration and GRN mutations: a genome-wide association study. (2018)
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/s1474-4422(18)30126-1
PubMed Identifier: 29724592
Publication URI: http://europepmc.org/abstract/MED/29724592
Type: Journal Article/Review
Volume: 17
Parent Publication: The Lancet. Neurology
Issue: 6
ISSN: 1474-4422