PINK1 mutation heterozygosity and the risk of Parkinson's disease.
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| Title: | PINK1 mutation heterozygosity and the risk of Parkinson's disease. |
|---|---|
| Authors: | Toft M (AUTHOR), Myhre R (AUTHOR), Pielsticker L (AUTHOR), White LR (AUTHOR), Aasly JO (AUTHOR), Farrer MJ (AUTHOR), Toft, M1 (AUTHOR), Myhre, R (AUTHOR), Pielsticker, L (AUTHOR), White, L R (AUTHOR), Aasly, J O (AUTHOR), Farrer, M J (AUTHOR) |
| Source: | Journal of Neurology, Neurosurgery & Psychiatry. Jan2007, Vol. 78 Issue 1, p82-84. 3p. |
| Database: | Academic Search Ultimate |
| FullText | Text: Availability: 0 |
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| Header | DbId: asn DbLabel: Academic Search Ultimate An: 106289287 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=106289287 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1136/jnnp.2006.097840 Languages: – Code: eng Text: English PhysicalDescription: Pagination: PageCount: 3 StartPage: 82 Titles: – TitleFull: PINK1 mutation heterozygosity and the risk of Parkinson's disease. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Toft M – PersonEntity: Name: NameFull: Myhre R – PersonEntity: Name: NameFull: Pielsticker L – PersonEntity: Name: NameFull: White LR – PersonEntity: Name: NameFull: Aasly JO – PersonEntity: Name: NameFull: Farrer MJ – PersonEntity: Name: NameFull: Toft, M – PersonEntity: Name: NameFull: Myhre, R – PersonEntity: Name: NameFull: Pielsticker, L – PersonEntity: Name: NameFull: White, L R – PersonEntity: Name: NameFull: Aasly, J O – PersonEntity: Name: NameFull: Farrer, M J IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 01 Text: Jan2007 Type: published Y: 2007 Identifiers: – Type: issn-print Value: 00223050 Numbering: – Type: volume Value: 78 – Type: issue Value: 1 Titles: – TitleFull: Journal of Neurology, Neurosurgery & Psychiatry Type: main |
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