Publication: Author Correction: Elucidating causative gene variants in hereditary Parkinson's disease in the Global Parkinson's Genetics Program (GP2).
datacite.rights | open.access | |
dc.contributor.author | Lange, Lara M | |
dc.contributor.author | Avenali, Micol | |
dc.contributor.author | Ellis, Melina | |
dc.contributor.author | Illarionova, Anastasia | |
dc.contributor.author | Keller Sarmiento, Ignacio J | |
dc.contributor.author | Tan, Ai-Huey | |
dc.contributor.author | Madoev, Harutyun | |
dc.contributor.author | Galandra, Caterina | |
dc.contributor.author | Junker, Johanna | |
dc.contributor.author | Roopnarain, Karisha | |
dc.contributor.author | Solle, Justin | |
dc.contributor.author | Wegel, Claire | |
dc.contributor.author | Fang, Zih-Hua | |
dc.contributor.author | Heutink, Peter | |
dc.contributor.author | Kumar, Kishore R | |
dc.contributor.author | Lim, Shen-Yang | |
dc.contributor.author | Valente, Enza Maria | |
dc.contributor.author | Nalls, Mike | |
dc.contributor.author | Blauwendraat, Cornelis | |
dc.contributor.author | Singleton, Andrew | |
dc.contributor.author | Mencacci, Niccolo | |
dc.contributor.author | Lohmann, Katja | |
dc.contributor.author | Klein, Christine | |
dc.date.accessioned | 2024-10-25T18:40:01Z | |
dc.date.available | 2024-10-25T18:40:01Z | |
dc.date.issued | 2023-09-13 | |
dc.description.note | Christiane Zweier is part of the Collaborators: Global Parkinson’s Genetic Program (GP2) | |
dc.identifier.doi | 10.48350/189661 | |
dc.identifier.pmid | 37704671 | |
dc.identifier.publisherDOI | 10.1038/s41531-023-00560-7 | |
dc.identifier.uri | https://boris-portal.unibe.ch/handle/20.500.12422/171881 | |
dc.language.iso | en | |
dc.publisher | Nature Publishing Group | |
dc.relation.ispartof | NPJ Parkinson's disease | |
dc.relation.issn | 2373-8057 | |
dc.relation.organization | A1656D321FF54C0CB48BA1262FBD5A0D | |
dc.subject.ddc | 600 - Technology::610 - Medicine & health | |
dc.title | Author Correction: Elucidating causative gene variants in hereditary Parkinson's disease in the Global Parkinson's Genetics Program (GP2). | |
dc.type | article | |
dspace.entity.type | Publication | |
dspace.file.type | text | |
oaire.citation.issue | 1 | |
oaire.citation.startPage | 133 | |
oaire.citation.volume | 9 | |
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unibe.date.licenseChanged | 2024-01-04 11:07:32 | |
unibe.description.ispublished | pub | |
unibe.eprints.legacyId | 189661 | |
unibe.refereed | true | |
unibe.subtype.article | contribution |
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