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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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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Bentham Science Publishers Ltd
2011
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3129042/ https://www.ncbi.nlm.nih.gov/pubmed/21886454 http://dx.doi.org/10.2174/138920211794520150 |