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Macular thickness changes in a patient with Leber’s hereditary optic neuropathy
BACKGROUND: Leber’s hereditary optic neuropathy (LHON) refers to an optic nerve dysfunction due to mutations in the mitochondrial DNA, resulting in visual loss by apoptosis of retinal ganglion cells (RGC). In 20% of LHON cases, their fundus examination looks entirely normal at early stage. There are...
Autores principales: | Mizoguchi, Ayako, Hashimoto, Yuki, Shinmei, Yasuhiro, Nozaki, Mayo, Ishijima, Kan, Tagawa, Yoshiaki, Ishida, Susumu |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4373513/ https://www.ncbi.nlm.nih.gov/pubmed/25885098 http://dx.doi.org/10.1186/s12886-015-0015-1 |
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