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Leber's hereditary optic neuropathy: Severe vascular pathology in a severe primary mutation
The purpose of the present article was to evaluate the previously unreported vascular alterations in Leber's Hereditary Optic Neuropathy (LHON) 3460 mitochondrial DNA (mtDNA) mutation. Among the three primary mtDNA mutations, namely 11778, 14484, and 3460, LHON 3460 is the most rare and histori...
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| Udgivet i: | Intractable Rare Dis Res |
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| Main Authors: | , , , , , |
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
International Research and Cooperation Association for Bio & Socio-Sciences Advancement
2019
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| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6409112/ https://ncbi.nlm.nih.gov/pubmed/30881859 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5582/irdr.2018.01126 |
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