Genetic variations in GBA1 and LRRK2 genes: Biochemical and clinical consequences in Parkinson disease.
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| Title: | Genetic variations in GBA1 and LRRK2 genes: Biochemical and clinical consequences in Parkinson disease. |
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| Authors: | Smith LJ; Department of Clinical and Movement Neurosciences, Queen Square Institute of Neurology, University College London (UCL), London, United Kingdom.; Aligning Science Across Parkinson's (ASAP) Collaborative Research Network, Chevy Chase, MD, United States., Lee CY; Department of Clinical and Movement Neurosciences, Queen Square Institute of Neurology, University College London (UCL), London, United Kingdom.; Aligning Science Across Parkinson's (ASAP) Collaborative Research Network, Chevy Chase, MD, United States., Menozzi E; Department of Clinical and Movement Neurosciences, Queen Square Institute of Neurology, University College London (UCL), London, United Kingdom.; Aligning Science Across Parkinson's (ASAP) Collaborative Research Network, Chevy Chase, MD, United States., Schapira AHV; Department of Clinical and Movement Neurosciences, Queen Square Institute of Neurology, University College London (UCL), London, United Kingdom.; Aligning Science Across Parkinson's (ASAP) Collaborative Research Network, Chevy Chase, MD, United States. |
| Source: | Frontiers in neurology [Front Neurol] 2022 Aug 12; Vol. 13, pp. 971252. Date of Electronic Publication: 2022 Aug 12 (Print Publication: 2022). |
| Publication Type: | Journal Article; Review |
| Journal Info: | Publisher: Frontiers Research Foundation Country of Publication: Switzerland NLM ID: 101546899 Publication Model: eCollection Cited Medium: Print ISSN: 1664-2295 (Print) Linking ISSN: 16642295 NLM ISO Abbreviation: Front Neurol Subsets: PubMed not MEDLINE |
| Database: | MEDLINE Ultimate |
| FullText | Links: – Type: pdflink Text: Availability: 0 |
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| Header | DbId: mdl DbLabel: MEDLINE Ultimate An: 36034282 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Genetic variations in GBA1 and LRRK2 genes: Biochemical and clinical consequences in Parkinson disease. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AU" term="%22Smith+LJ%22">Smith LJ</searchLink>; Department of Clinical and Movement Neurosciences, Queen Square Institute of Neurology, University College London (UCL), London, United Kingdom.; Aligning Science Across Parkinson's (ASAP) Collaborative Research Network, Chevy Chase, MD, United States.<br /><searchLink fieldCode="AU" term="%22Lee+CY%22">Lee CY</searchLink>; Department of Clinical and Movement Neurosciences, Queen Square Institute of Neurology, University College London (UCL), London, United Kingdom.; Aligning Science Across Parkinson's (ASAP) Collaborative Research Network, Chevy Chase, MD, United States.<br /><searchLink fieldCode="AU" term="%22Menozzi+E%22">Menozzi E</searchLink>; Department of Clinical and Movement Neurosciences, Queen Square Institute of Neurology, University College London (UCL), London, United Kingdom.; Aligning Science Across Parkinson's (ASAP) Collaborative Research Network, Chevy Chase, MD, United States.<br /><searchLink fieldCode="AU" term="%22Schapira+AHV%22">Schapira AHV</searchLink>; Department of Clinical and Movement Neurosciences, Queen Square Institute of Neurology, University College London (UCL), London, United Kingdom.; Aligning Science Across Parkinson's (ASAP) Collaborative Research Network, Chevy Chase, MD, United States. – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%22101546899%22">Frontiers in neurology</searchLink> [Front Neurol] 2022 Aug 12; Vol. 13, pp. 971252. <i>Date of Electronic Publication: </i>2022 Aug 12 (<i>Print Publication: </i>2022). – Name: TypePub Label: Publication Type Group: TypPub Data: Journal Article; Review – Name: TitleSource Label: Journal Info Group: Src Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Frontiers+Research+Foundation%22">Frontiers Research Foundation </searchLink><i>Country of Publication: </i>Switzerland <i>NLM ID: </i>101546899 <i>Publication Model: </i>eCollection <i>Cited Medium: </i>Print <i>ISSN: </i>1664-2295 (Print) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2216642295%22">16642295 </searchLink><i>NLM ISO Abbreviation: </i>Front Neurol <i>Subsets: </i>PubMed not MEDLINE |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=mdl&AN=36034282 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.3389/fneur.2022.971252 Languages: – Code: eng Text: English PhysicalDescription: Pagination: StartPage: 971252 Titles: – TitleFull: Genetic variations in GBA1 and LRRK2 genes: Biochemical and clinical consequences in Parkinson disease. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Smith LJ – PersonEntity: Name: NameFull: Lee CY – PersonEntity: Name: NameFull: Menozzi E – PersonEntity: Name: NameFull: Schapira AHV IsPartOfRelationships: – BibEntity: Dates: – D: 12 M: 08 Text: 2022 Aug 12 Type: published Y: 2022 Identifiers: – Type: issn-print Value: 1664-2295 Numbering: – Type: volume Value: 13 Titles: – TitleFull: Frontiers in neurology Type: main |
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