טוען...
Frequency of primary mutations of Leber's hereditary optic neuropathy patients in North Indian population
PURPOSE: Leber's hereditary optic neuropathy (LHON) is an inherited optic neuropathy characterized by subacute painless vision loss. The majority of LHON is caused due to one of the three primary mutations in the mitochondrial DNA (m.G3460A, m.G11778A, and m.T14484C). The frequency of these mut...
שמור ב:
| הוצא לאור ב: | Indian J Ophthalmol |
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| Main Authors: | , , , , , |
| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
Medknow Publications & Media Pvt Ltd
2017
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| נושאים: | |
| גישה מקוונת: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5700584/ https://ncbi.nlm.nih.gov/pubmed/29133642 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/ijo.IJO_380_17 |
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