Whole mitochondrial genome sequencing in individuals with Leber hereditary optic neuropathy negative for the common pathogenic mitochondrial DNA variants.
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| Title: | Whole mitochondrial genome sequencing in individuals with Leber hereditary optic neuropathy negative for the common pathogenic mitochondrial DNA variants. |
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| Authors: | Srilekha S; SNONGC Department of Genetics and Molecular Biology, Medical Research Foundation, Chennai, India., Ambika S; Department of Neuro-Ophthalmology, Medical Research Foundation, Chennai, India., Hemavathy N; Vision Research Foundation, Centre for Bioinformatics, Chennai, India., Vidhya D; Department of Neuro-Ophthalmology, Medical Research Foundation, Chennai, India., Yu-Wai-Man P; John van Geest Centre for Brain Repair and MRC Mitochondrial Biology Unit, Department of Clinical Neurosciences, University of Cambridge, Cambridge, United Kingdom.; Cambridge Eye Unit, Addenbrooke's Hospital, Cambridge University Hospitals NHS Foundation Trust, Cambridge, United Kingdom.; Moorfields Eye Hospital NHS Foundation Trust, London, United Kingdom.; Institute of Ophthalmology, University College London, London, United Kingdom. |
| Source: | Frontiers in neurology [Front Neurol] 2025 Sep 01; Vol. 16, pp. 1584748. Date of Electronic Publication: 2025 Sep 01 (Print Publication: 2025). |
| Publication Type: | Journal Article |
| 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 |
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| FullText | Links: – Type: pdflink Text: Availability: 1 |
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| Header | DbId: mdl DbLabel: MEDLINE Ultimate An: 40969215 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Whole mitochondrial genome sequencing in individuals with Leber hereditary optic neuropathy negative for the common pathogenic mitochondrial DNA variants. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AU" term="%22Srilekha+S%22">Srilekha S</searchLink>; SNONGC Department of Genetics and Molecular Biology, Medical Research Foundation, Chennai, India.<br /><searchLink fieldCode="AU" term="%22Ambika+S%22">Ambika S</searchLink>; Department of Neuro-Ophthalmology, Medical Research Foundation, Chennai, India.<br /><searchLink fieldCode="AU" term="%22Hemavathy+N%22">Hemavathy N</searchLink>; Vision Research Foundation, Centre for Bioinformatics, Chennai, India.<br /><searchLink fieldCode="AU" term="%22Vidhya+D%22">Vidhya D</searchLink>; Department of Neuro-Ophthalmology, Medical Research Foundation, Chennai, India.<br /><searchLink fieldCode="AU" term="%22Yu-Wai-Man+P%22">Yu-Wai-Man P</searchLink>; John van Geest Centre for Brain Repair and MRC Mitochondrial Biology Unit, Department of Clinical Neurosciences, University of Cambridge, Cambridge, United Kingdom.; Cambridge Eye Unit, Addenbrooke's Hospital, Cambridge University Hospitals NHS Foundation Trust, Cambridge, United Kingdom.; Moorfields Eye Hospital NHS Foundation Trust, London, United Kingdom.; Institute of Ophthalmology, University College London, London, United Kingdom. – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%22101546899%22">Frontiers in neurology</searchLink> [Front Neurol] 2025 Sep 01; Vol. 16, pp. 1584748. <i>Date of Electronic Publication: </i>2025 Sep 01 (<i>Print Publication: </i>2025). – Name: TypePub Label: Publication Type Group: TypPub Data: Journal Article – 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=40969215 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.3389/fneur.2025.1584748 Languages: – Code: eng Text: English PhysicalDescription: Pagination: StartPage: 1584748 Titles: – TitleFull: Whole mitochondrial genome sequencing in individuals with Leber hereditary optic neuropathy negative for the common pathogenic mitochondrial DNA variants. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Srilekha S – PersonEntity: Name: NameFull: Ambika S – PersonEntity: Name: NameFull: Hemavathy N – PersonEntity: Name: NameFull: Vidhya D – PersonEntity: Name: NameFull: Yu-Wai-Man P IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 09 Text: 2025 Sep 01 Type: published Y: 2025 Identifiers: – Type: issn-print Value: 1664-2295 Numbering: – Type: volume Value: 16 Titles: – TitleFull: Frontiers in neurology Type: main |
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