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)


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