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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| ISSN: | 1664-2295 |
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| DOI: | 10.3389/fneur.2025.1584748 |
