OUTER RETINAL DYSFUNCTION IN A PATIENT WITH THE 15257 MITOCHONDRIAL DNA MUTATION
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
Ophthalmology,General Medicine
Reference8 articles.
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2. Novel mtDNA mutations and oxidative phosphorylation dysfunction in Russian LHON families.;Brown;Hum Genet,2001
3. Mitochondrial DNA complex I and III mutations associated with Lebers hereditary optic neuropathy.;Brown;Genetics,1992
4. Lebers hereditary optic neuropathy: the etiological role of a mutation in the mitochondrial cytochrome b gene.;Howell;Genetics,1993
5. Lebers hereditary optic neuropathy. Clinical manifestations of the 15257 mutation.;Johns;Ophthalmology,1993
Cited by 2 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Leber Hereditary Optic Neuropathy With Childhood Onset Producing Severe Unilateral Optic Neuropathy With No Relative Afferent Pupillary Defect;Journal of Neuro-Ophthalmology;2022-07-08
2. Unilateral cone-rod dysfunction and retinal thinning in a child carrying the 14484 mutation of Leber hereditary optic neuropathy;Journal of American Association for Pediatric Ophthalmology and Strabismus;2019-04
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