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The Prevalence and Natural History of Dominant Optic Atrophy due to OPA1 Mutations
PURPOSE: Autosomal dominant optic atrophy (DOA) is a major cause of visual impairment in young adults and it is characterized by selective retinal ganglion cell loss. In order to define the prevalence and natural history of this optic nerve disorder, we performed a population-based epidemiological a...
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| Main Authors: | , , , , , , , , , , , |
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| Formáid: | Artigo |
| Teanga: | Inglês |
| Foilsithe: |
2010
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| Ábhair: | |
| Rochtain Ar Líne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4040407/ https://ncbi.nlm.nih.gov/pubmed/20417570 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ophtha.2009.12.038 |
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