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Author Correction: common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology (Nature Genetics, (2021), 53, 12, (1636-1648), 10.1038/s41588-021-00973-1)

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dc.contributor.coauthorvan Rheenen, Wouter
dc.contributor.coauthorvan der Spek, Rick A. A.
dc.contributor.coauthorBakker, Mark K.
dc.contributor.coauthorvan Vugt, Joke J. F. A.
dc.contributor.coauthorHop, Paul J.
dc.contributor.coauthorZwamborn, Ramona A. J.
dc.contributor.coauthorde Klein, Niek
dc.contributor.coauthorWestra, Harm-Jan
dc.contributor.coauthorBakker, Olivier B.
dc.contributor.coauthorDeelen, Patrick
dc.contributor.coauthorRestuadi, Restuadi
dc.contributor.coauthorGawor, Klara
dc.contributor.coauthorWesteneng, Henk-Jan
dc.contributor.coauthorvan Eijk, Kristel R.
dc.contributor.coauthorAl Khleifat, Ahmad
dc.contributor.coauthorTicozzi, Nicola
dc.contributor.coauthorCooper-Knock, Johnathan
dc.contributor.coauthorGromicho, Marta
dc.contributor.coauthorChandran, Siddharthan
dc.contributor.coauthorOrrell, Richard W.
dc.contributor.coauthorSendtner, Michael
dc.contributor.coauthorCereda, Cristina
dc.contributor.coauthorSproviero, Daisy
dc.contributor.coauthorRatti, Antonia
dc.contributor.coauthorSiciliano, Gabriele
dc.contributor.coauthorFilosto, Massimiliano
dc.contributor.coauthorMoglia, Cristina
dc.contributor.coauthorGrassano, Maurizio
dc.contributor.coauthorBeghi, Ettor
dc.contributor.coauthorOsmanovic, Alma
dc.contributor.coauthorLerner, Yossef
dc.contributor.coauthorZabari, Michal
dc.contributor.coauthorNefussy, Beatrice
dc.contributor.coauthorMora Pardina, Jesus S.
dc.contributor.coauthorDion, Patrick A.
dc.contributor.coauthorBensimon, Gilbert
dc.contributor.coauthorOlsen, Catherine M.
dc.contributor.coauthorCeroni, Mauro
dc.contributor.coauthorDiamanti, Luca
dc.contributor.coauthorFerrarese, Carlo
dc.contributor.coauthorTremolizzo, Lucio
dc.contributor.coauthorTorrieri, Maria Claudia
dc.contributor.coauthorBombaci, Alessandro
dc.contributor.coauthorMazzini, Letizia
dc.contributor.coauthorCorrado, Lucia
dc.contributor.coauthorDe Mattei, Marco
dc.contributor.departmentSchool of Medicine
dc.contributor.kuauthorBaşak, Ayşe Nazlı
dc.contributor.schoolcollegeinstituteSCHOOL OF MEDICINE
dc.date.accessioned2024-11-09T23:59:22Z
dc.date.issued2022
dc.description.abstractIn the version of this article initially published, the affiliation for Nazli Başak appeared incorrectly. Nazli Başak is at Koç University, School of Medicine, KUTTAM-NDAL, Istanbul, Turkey, and not Bogazici University. The error has been corrected in the HTML and PDF versions of the article. © 2022, The Author(s).
dc.description.indexedbyScopus
dc.description.indexedbyPubMed
dc.description.issue3
dc.description.openaccessYES
dc.description.publisherscopeInternational
dc.description.sponsoredbyTubitakEuN/A
dc.description.volume54
dc.identifier.doi10.1038/s41588-022-01020-3
dc.identifier.issn1061-4036
dc.identifier.scopus2-s2.0-85124104874
dc.identifier.urihttps://doi.org/10.1038/s41588-022-01020-3
dc.identifier.urihttps://hdl.handle.net/20.500.14288/15630
dc.keywordsErratum
dc.language.isoeng
dc.publisherNature Research
dc.relation.ispartofNature Genetics
dc.subjectGenetics
dc.subjectHeredity
dc.titleAuthor Correction: common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology (Nature Genetics, (2021), 53, 12, (1636-1648), 10.1038/s41588-021-00973-1)
dc.typeOther
dc.type.otherErratum
dspace.entity.typePublication
local.contributor.kuauthorBaşak, Ayşe Nazlı
local.publication.orgunit1SCHOOL OF MEDICINE
local.publication.orgunit2School of Medicine
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relation.isParentOrgUnitOfPublication17f2dc8e-6e54-4fa8-b5e0-d6415123a93e
relation.isParentOrgUnitOfPublication.latestForDiscovery17f2dc8e-6e54-4fa8-b5e0-d6415123a93e

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