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LHON: Mitochondrial Mutations and More
Leber’s hereditary optic neuropathy (LHON) is a mitochondrial disorder leading to severe visual impairment or even blindness by death of retinal ganglion cells (RGCs). The primary cause of the disease is usually a mutation of the mitochondrial genome (mtDNA) causing a single amino acid exchange in o...
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| Autor principal: | |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Bentham Science Publishers Ltd
2011
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| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3129042/ https://ncbi.nlm.nih.gov/pubmed/21886454 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2174/138920211794520150 |
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