A systematic review of associations between common SNCA variants and clinical heterogeneity in Parkinson's disease
| dc.contributor.author | Pedersen, Camilla Christina | |
| dc.contributor.author | Lange, Johannes | |
| dc.contributor.author | Forland, Marthe Gurine Gunnarsdatter | |
| dc.contributor.author | Macleod, Angus D. | |
| dc.contributor.author | Alves, Guido | |
| dc.contributor.author | Maple-Grodem, Jodi | |
| dc.contributor.institution | University of Aberdeen.Medicine, Medical Sciences & Nutrition | en |
| dc.contributor.institution | University of Aberdeen.Other Applied Health Sciences | en |
| dc.date.accessioned | 2021-09-29T15:37:01Z | |
| dc.date.available | 2021-09-29T15:37:01Z | |
| dc.date.issued | 2021-07-01 | |
| dc.description | ACKNOWLEDGEMENTS C.C.P. is supported by HELSEVEST (29604). M.G.G.F. is supported by The National Association for Public Health (16152). J.M.-G. and G.A. are supported by the Research Council of Norway (287842). | en |
| dc.description.status | Peer reviewed | en |
| dc.format.extent | 10 | |
| dc.format.extent | 1167358 | |
| dc.identifier | 194372280 | |
| dc.identifier | 02fc9701-0d9f-44fd-9034-2d7f1bc5e20e | |
| dc.identifier | 000668887100001 | |
| dc.identifier | 34210990 | |
| dc.identifier | 000668887100001 | |
| dc.identifier | 85109165714 | |
| dc.identifier.citation | Pedersen, C C, Lange, J, Forland, M G G, Macleod, A D, Alves, G & Maple-Grodem, J 2021, 'A systematic review of associations between common SNCA variants and clinical heterogeneity in Parkinson's disease', npj Parkinson's Disease, vol. 7 , 54. https://doi.org/10.1038/s41531-021-00196-5 | en |
| dc.identifier.doi | 10.1038/s41531-021-00196-5 | |
| dc.identifier.issn | 2373-8057 | |
| dc.identifier.other | PubMedCentral: PMC8249472 | |
| dc.identifier.uri | https://hdl.handle.net/2164/17217 | |
| dc.identifier.vol | 7 | en |
| dc.language.iso | eng | |
| dc.relation.ispartof | npj Parkinson's Disease | en |
| dc.subject | SDG 3 - Good Health and Well-being | en |
| dc.subject | ALPHA-SYNUCLEIN GENE | en |
| dc.subject | INCREASES RISK | en |
| dc.subject | POLYMORPHISM | en |
| dc.subject | PROGRESSION | en |
| dc.subject | SYMPTOMS | en |
| dc.subject | PROMOTER | en |
| dc.subject | TAU | en |
| dc.subject | AGE | en |
| dc.subject | DUPLICATION | en |
| dc.subject | VARIABILITY | en |
| dc.subject | R Medicine | en |
| dc.subject | Supplementary Information | en |
| dc.subject | https://doi.org/10.1038/s41531-021-00196-5 | en |
| dc.subject.lcc | R | en |
| dc.title | A systematic review of associations between common SNCA variants and clinical heterogeneity in Parkinson's disease | en |
| dc.type | Journal item | en |
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