Correction: Whole-genome sequencing analysis reveals new susceptibility loci and structural variants associated with progressive supranuclear palsy

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dc.contributor.authorWang, Hui
dc.contributor.authorChang, Timothy S.
dc.contributor.authorDombroski, Beth A.
dc.contributor.authorCheng, Po-Liang
dc.contributor.authorPatil, Vishakha
dc.contributor.authorValiente-Banuet, Leopoldo
dc.contributor.authorFarrell, Kurt
dc.contributor.authorMclean, Catriona
dc.contributor.authorMolina-Porcel, Laura
dc.contributor.authorRajput, Alex
dc.contributor.authorDe Deyn, Peter Paul
dc.contributor.authorLe Bastard, Nathalie
dc.contributor.authorGearing, Marla
dc.contributor.authorDonker Kaat, Laura
dc.contributor.authorVan Swieten, John C.
dc.contributor.authorDopper, Elise
dc.contributor.authorGhetti, Bernardino F.
dc.contributor.authorNewell, Kathy L.
dc.contributor.authorTroakes, Claire
dc.contributor.authorde Yébenes, Justo G.
dc.contributor.authorRábano-Gutierrez, Alberto
dc.contributor.authorMeller, Tina
dc.contributor.authorOertel, Wolfgang H.
dc.contributor.authorRespondek, Gesine
dc.contributor.authorStamelou, Maria
dc.contributor.authorArzberger, Thomas
dc.contributor.authorRoeber, Sigrun
dc.contributor.authorMüller, Ulrich
dc.contributor.authorHopfner, Franziska
dc.contributor.authorPastor, Pau
dc.contributor.authorBrice, Alexis
dc.contributor.authorDurr, Alexandra
dc.contributor.authorLe Ber, Isabelle
dc.contributor.authorBeach, Thomas G.
dc.contributor.authorSerrano, Geidy E.
dc.contributor.authorHazrati, Lili-Naz
dc.contributor.authorLitvan, Irene
dc.contributor.authorRademakers, Rosa
dc.contributor.authorRoss, Owen A.
dc.contributor.authorGalasko, Douglas
dc.contributor.authorBoxer, Adam L.
dc.contributor.authorMiller, Bruce L.
dc.contributor.authorSeeley, Willian W.
dc.contributor.authorVan Deerlin, Vivanna M.
dc.contributor.authorLee, Edward B.
dc.contributor.authorWhite, Charles L., III
dc.contributor.authorMorris, Huw
dc.contributor.authorde Silva, Rohan
dc.contributor.authorCrary, John F.
dc.contributor.authorGoate, Alison M.
dc.contributor.authorFriedman, Jeffrey S.
dc.contributor.authorLeung, Yuk Yee
dc.contributor.authorCoppola, Giovanni
dc.contributor.authorNaj, Adam C.
dc.contributor.authorWang, Li-San
dc.contributor.authorP. S. P. genetics study group
dc.contributor.authorDalgard, Clifton
dc.contributor.authorDickson, Dennis W.
dc.contributor.authorHöglinger, Günter U.
dc.contributor.authorSchellenberg, Gerard D.
dc.contributor.authorGeschwind, Daniel H.
dc.contributor.authorLee, Wan-Ping
dc.contributor.departmentPathology and Laboratory Medicine, School of Medicine
dc.date.accessioned2024-11-19T08:49:07Z
dc.date.available2024-11-19T08:49:07Z
dc.date.issued2024-10-14
dc.description.abstractCorrection : Mol Neurodegeneration 19, 61 (2024) https://doi.org/10.1186/s13024-024-00747-3 The original article [1] erroneously gives a wrong affiliation for Ulrich Müller. His correct affiliation is Institute of Human Genetics, Justus-Liebig University Giessen, 35392 Giessen, Germany.
dc.eprint.versionFinal published version
dc.identifier.citationWang H, Chang TS, Dombroski BA, et al. Correction: Whole-genome sequencing analysis reveals new susceptibility loci and structural variants associated with progressive supranuclear palsy. Mol Neurodegener. 2024;19(1):73. Published 2024 Oct 14. doi:10.1186/s13024-024-00763-3
dc.identifier.urihttps://hdl.handle.net/1805/44603
dc.language.isoen_US
dc.publisherSpringer Nature
dc.relation.isversionof10.1186/s13024-024-00763-3
dc.relation.journalMolecular Neurodegeneration
dc.rightsAttribution 4.0 Internationalen
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.sourcePMC
dc.subjectProgressive Supranuclear Palsy (PSP)
dc.subjectWhole-Genome Sequencing (WGS)
dc.subjectGenome-Wide Association Study (GWAS)
dc.subjectStructural Variants (SVs)
dc.subjectApolipoprotein E (APOE)
dc.titleCorrection: Whole-genome sequencing analysis reveals new susceptibility loci and structural variants associated with progressive supranuclear palsy
dc.typeArticle
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