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Leber hereditary optic neuropathy: bridging the translational gap
PURPOSE OF REVIEW: Leber hereditary optic neuropathy (LHON) is the most common primary mitochondrial DNA (mtDNA) genetic disorder in the population. We address the clinical evolution of the disease, the secondary etiological factors that could contribute to visual loss, and the challenging task of d...
Uloženo v:
| Vydáno v: | Curr Opin Ophthalmol |
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| Hlavní autoři: | , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Lippincott Williams & Wilkins
2017
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5562441/ https://ncbi.nlm.nih.gov/pubmed/28650878 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1097/ICU.0000000000000410 |
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