Inherited mtDNA variations are not strong risk factors in human prion disease.
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| Title: | Inherited mtDNA variations are not strong risk factors in human prion disease. |
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| Authors: | Hudson G; Wellcome Trust Centre for Mitochondrial Research, Institute of Genetic Medicine, Newcastle University, UK., Uphill J; MRC Prion Unit, Department of Neurodegenerative Disease, UCL Institute of Neurology, London, UK., Hummerich H; MRC Prion Unit, Department of Neurodegenerative Disease, UCL Institute of Neurology, London, UK., Blevins J; Department of Pathology, Case Western Reserve University, Cleveland, OH, USA., Gambetti P; Department of Pathology, Case Western Reserve University, Cleveland, OH, USA., Zerr I; Clinical Dementia Center, Department of Neurology, Georg-August University Göttingen, Göttingen, Germany; Center for Neuropathology and Prion Research, Ludwig-Maximilians-University Munich Munich, Germany., Collinge J; MRC Prion Unit, Department of Neurodegenerative Disease, UCL Institute of Neurology, London, UK., Mead S; MRC Prion Unit, Department of Neurodegenerative Disease, UCL Institute of Neurology, London, UK. Electronic address: s.mead@prion.ucl.ac.uk., Chinnery PF; Wellcome Trust Centre for Mitochondrial Research, Institute of Genetic Medicine, Newcastle University, UK. |
| Source: | Neurobiology of aging [Neurobiol Aging] 2015 Oct; Vol. 36 (10), pp. 2908.e1-3. Date of Electronic Publication: 2015 Jul 10. |
| Publication Type: | Journal Article; Research Support, Non-U.S. Gov't |
| Journal Info: | Publisher: Elsevier Country of Publication: United States NLM ID: 8100437 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1558-1497 (Electronic) Linking ISSN: 01974580 NLM ISO Abbreviation: Neurobiol Aging Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
| FullText | Text: Availability: 0 |
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| Header | DbId: mdl DbLabel: MEDLINE Ultimate An: 26239179 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Inherited mtDNA variations are not strong risk factors in human prion disease. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AU" term="%22Hudson+G%22">Hudson G</searchLink>; Wellcome Trust Centre for Mitochondrial Research, Institute of Genetic Medicine, Newcastle University, UK.<br /><searchLink fieldCode="AU" term="%22Uphill+J%22">Uphill J</searchLink>; MRC Prion Unit, Department of Neurodegenerative Disease, UCL Institute of Neurology, London, UK.<br /><searchLink fieldCode="AU" term="%22Hummerich+H%22">Hummerich H</searchLink>; MRC Prion Unit, Department of Neurodegenerative Disease, UCL Institute of Neurology, London, UK.<br /><searchLink fieldCode="AU" term="%22Blevins+J%22">Blevins J</searchLink>; Department of Pathology, Case Western Reserve University, Cleveland, OH, USA.<br /><searchLink fieldCode="AU" term="%22Gambetti+P%22">Gambetti P</searchLink>; Department of Pathology, Case Western Reserve University, Cleveland, OH, USA.<br /><searchLink fieldCode="AU" term="%22Zerr+I%22">Zerr I</searchLink>; Clinical Dementia Center, Department of Neurology, Georg-August University Göttingen, Göttingen, Germany; Center for Neuropathology and Prion Research, Ludwig-Maximilians-University Munich Munich, Germany.<br /><searchLink fieldCode="AU" term="%22Collinge+J%22">Collinge J</searchLink>; MRC Prion Unit, Department of Neurodegenerative Disease, UCL Institute of Neurology, London, UK.<br /><searchLink fieldCode="AU" term="%22Mead+S%22">Mead S</searchLink>; MRC Prion Unit, Department of Neurodegenerative Disease, UCL Institute of Neurology, London, UK. Electronic address: s.mead@prion.ucl.ac.uk.<br /><searchLink fieldCode="AU" term="%22Chinnery+PF%22">Chinnery PF</searchLink>; Wellcome Trust Centre for Mitochondrial Research, Institute of Genetic Medicine, Newcastle University, UK. – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%228100437%22">Neurobiology of aging</searchLink> [Neurobiol Aging] 2015 Oct; Vol. 36 (10), pp. 2908.e1-3. <i>Date of Electronic Publication: </i>2015 Jul 10. – Name: TypePub Label: Publication Type Group: TypPub Data: Journal Article; Research Support, Non-U.S. Gov't – Name: TitleSource Label: Journal Info Group: Src Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Elsevier%22">Elsevier </searchLink><i>Country of Publication: </i>United States <i>NLM ID: </i>8100437 <i>Publication Model: </i>Print-Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>1558-1497 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2201974580%22">01974580 </searchLink><i>NLM ISO Abbreviation: </i>Neurobiol Aging <i>Subsets: </i>MEDLINE |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=mdl&AN=26239179 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1016/j.neurobiolaging.2015.07.005 Languages: – Code: eng Text: English PhysicalDescription: Pagination: StartPage: 2908.e1-3 Titles: – TitleFull: Inherited mtDNA variations are not strong risk factors in human prion disease. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Hudson G – PersonEntity: Name: NameFull: Uphill J – PersonEntity: Name: NameFull: Hummerich H – PersonEntity: Name: NameFull: Blevins J – PersonEntity: Name: NameFull: Gambetti P – PersonEntity: Name: NameFull: Zerr I – PersonEntity: Name: NameFull: Collinge J – PersonEntity: Name: NameFull: Mead S – PersonEntity: Name: NameFull: Chinnery PF IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 10 Text: 2015 Oct Type: published Y: 2015 Identifiers: – Type: issn-electronic Value: 1558-1497 Numbering: – Type: volume Value: 36 – Type: issue Value: 10 Titles: – TitleFull: Neurobiology of aging Type: main |
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