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: Yu-Wai-Man, Patrick, Griffiths, Philip G., Burke, Ailbhe, Sellar, Peter W., Clarke, Michael P., Gnanaraj, Lawrence, Ah-Kine, Desiree, Hudson, Gavin, Czermin, Birgit, Taylor, Robert W., Horvath, Rita, Chinnery, Patrick F.
Formato: Artigo
Idioma:Inglês
Publicado em: 2010
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Article
Acesso em linha: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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