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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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| Publicado no: | Clin Ophthalmol |
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| Main Authors: | , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Dove Medical Press
2016
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| Assuntos: | |
| Acesso em linha: | 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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