טוען...
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...
שמור ב:
| הוצא לאור ב: | Invest Ophthalmol Vis Sci |
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| Main Authors: | , , , , , , , , |
| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
2008
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| נושאים: | |
| גישה מקוונת: | 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 |
| תגים: |
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