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Genetic variation in PLEKHG1 is associated with white matter hyperintensities (n = 11,226). (2019)

First Author: Traylor M

Attributed to: UK Biobank (core renewal) funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1212/wnl.0000000000006952

PubMed Identifier: 30659137

Publication URI: http://europepmc.org/abstract/MED/30659137

Type: Journal Article/Review

Volume: 92

Parent Publication: Neurology

Issue: 8

ISSN: 0028-3878