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dc.contributor.authorArmstrong, Nicola J
dc.contributor.authorMather, Karen A.
dc.contributor.authorSargurupremraj, Muralidharan
dc.contributor.authorKnol, Maria J.
dc.contributor.authorMalik, Rainer
dc.contributor.authorSatizabal, Claudia L.
dc.contributor.authorYanek, Lisa R.
dc.contributor.authorWen, Wei
dc.contributor.authorGudnason, Vilmundur G.
dc.contributor.authorDueker, Nicole D.
dc.contributor.authorElliott, Lloyd T.
dc.contributor.authorHofer, Edith
dc.contributor.authorHåberg, Asta
dc.contributor.authorJahanshad, Neda
dc.contributor.authorNyquist, Paul A.
dc.date.accessioned2022-03-01T14:25:07Z
dc.date.available2022-03-01T14:25:07Z
dc.date.created2021-02-03T16:56:19Z
dc.date.issued2020
dc.identifier.issn0039-2499
dc.identifier.urihttps://hdl.handle.net/11250/2982170
dc.language.isoengen_US
dc.titleCommon Genetic Variation Indicates Separate Causes for Periventricular and Deep White Matter Hyperintensitiesen_US
dc.typeJournal articleen_US
dc.typePeer revieweden_US
dc.description.versionpublishedVersionen_US
dc.rights.holderThe published version of the article will not be available due to copyright restrictionsen_US
dc.source.journalStrokeen_US
dc.identifier.doi10.1161/STROKEAHA.119.027544
dc.identifier.cristin1886448
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode2


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