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Leber’s hereditary optic neuropathy is multiorgan not mono-organ
Leber’s hereditary optic neuropathy (LHON) is a maternally inherited mitochondrial disorder with bilateral loss of central vision primarily due to mitochondrial DNA (mtDNA) mutations in subunits of complex I in the respiratory chain (primary LHON mutations), while other mtDNA mutations can also be c...
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| 出版年: | Clin Ophthalmol |
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| 主要な著者: | , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Dove Medical Press
2016
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5098596/ https://ncbi.nlm.nih.gov/pubmed/27843288 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2147/OPTH.S120197 |
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