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Adaptive Optics Scanning Laser Ophthalmoscopy Images in a Family with the Mitochondrial DNA T8993C Mutation

PURPOSE: This study was designed to assess the effect of mitochondrial DNA (mtDNA) mutation T8993C on cone structure in a family expressing neurogenic muscle weakness, ataxia, and retinitis pigmentosa (NARP) syndrome. METHODS: Five family members were studied, using clinical examination, nerve condu...

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Publicat a:Invest Ophthalmol Vis Sci
Autors principals: Yoon, Michael K., Roorda, Austin, Zhang, Yuhua, Nakanishi, Chiaki, Wong, Lee-Jun C., Zhang, Qing, Gillum, Leslie, Green, Ari, Duncan, Jacque L.
Format: Artigo
Idioma:Inglês
Publicat: 2008
Matèries:
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC4836613/
https://ncbi.nlm.nih.gov/pubmed/18997096
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1167/iovs.08-2029
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