A mitochondrial DNA tRNA(Val) point mutation associated with adult-onset Leigh syndrome.
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| Title: | A mitochondrial DNA tRNA(Val) point mutation associated with adult-onset Leigh syndrome. |
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| Authors: | Chalmers RM; Neurogenetics Section, University Department of Clinical Neurology, Queen Square, London, UK., Lamont PJ, Nelson I, Ellison DW, Thomas NH, Harding AE, Hammans SR |
| Source: | Neurology [Neurology] 1997 Aug; Vol. 49 (2), pp. 589-92. |
| Publication Type: | Case Reports; Journal Article; Research Support, Non-U.S. Gov't |
| Journal Info: | Publisher: Lippincott Williams & Wilkins Country of Publication: United States NLM ID: 0401060 Publication Model: Print Cited Medium: Print ISSN: 0028-3878 (Print) Linking ISSN: 00283878 NLM ISO Abbreviation: Neurology Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
| FullText | Text: Availability: 0 |
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| Header | DbId: mdl DbLabel: MEDLINE Ultimate An: 9270602 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: A mitochondrial DNA tRNA(Val) point mutation associated with adult-onset Leigh syndrome. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AU" term="%22Chalmers+RM%22">Chalmers RM</searchLink>; Neurogenetics Section, University Department of Clinical Neurology, Queen Square, London, UK.<br /><searchLink fieldCode="AU" term="%22Lamont+PJ%22">Lamont PJ</searchLink><br /><searchLink fieldCode="AU" term="%22Nelson+I%22">Nelson I</searchLink><br /><searchLink fieldCode="AU" term="%22Ellison+DW%22">Ellison DW</searchLink><br /><searchLink fieldCode="AU" term="%22Thomas+NH%22">Thomas NH</searchLink><br /><searchLink fieldCode="AU" term="%22Harding+AE%22">Harding AE</searchLink><br /><searchLink fieldCode="AU" term="%22Hammans+SR%22">Hammans SR</searchLink> – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%220401060%22">Neurology</searchLink> [Neurology] 1997 Aug; Vol. 49 (2), pp. 589-92. – Name: TypePub Label: Publication Type Group: TypPub Data: Case Reports; Journal Article; Research Support, Non-U.S. Gov't – Name: TitleSource Label: Journal Info Group: Src Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Lippincott+Williams+%26+Wilkins%22">Lippincott Williams & Wilkins </searchLink><i>Country of Publication: </i>United States <i>NLM ID: </i>0401060 <i>Publication Model: </i>Print <i>Cited Medium: </i>Print <i>ISSN: </i>0028-3878 (Print) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2200283878%22">00283878 </searchLink><i>NLM ISO Abbreviation: </i>Neurology <i>Subsets: </i>MEDLINE |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=mdl&AN=9270602 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1212/wnl.49.2.589 Languages: – Code: eng Text: English PhysicalDescription: Pagination: StartPage: 589 Titles: – TitleFull: A mitochondrial DNA tRNA(Val) point mutation associated with adult-onset Leigh syndrome. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Chalmers RM – PersonEntity: Name: NameFull: Lamont PJ – PersonEntity: Name: NameFull: Nelson I – PersonEntity: Name: NameFull: Ellison DW – PersonEntity: Name: NameFull: Thomas NH – PersonEntity: Name: NameFull: Harding AE – PersonEntity: Name: NameFull: Hammans SR IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 08 Text: 1997 Aug Type: published Y: 1997 Identifiers: – Type: issn-print Value: 0028-3878 Numbering: – Type: volume Value: 49 – Type: issue Value: 2 Titles: – TitleFull: Neurology Type: main |
| ResultId | 1 |