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Retinal Sublayer Thickness Analysis of The Macula of Symptomatic and Asymptomatic Carriers of G11778A Mutations with Leber's Hereditary Optic Neuropathy

2022-03-18

Abstract excerpt

<h4>Background: </h4> Leber's hereditary optic neuropathy (LHON) is a maternally inherited mitochondrial genetic disease, caused mainly by G11778A mutations. Analysis of retinal sublayer structure by spectral domain optical coherence tomography(SD-OCT) is of great significance for elucidating the pathogenesis of LHON. Purpose To analyze the thicknesses of the outer plexiform layer (OPL), outer nuclear layer (ONL)...

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Literature Corpus work
8aea3b00-d150-5d82-b9f2-93dc63e228ed
DOI
10.21203/rs.3.rs-1454379/v1
Open publication

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Retinal Sublayer Thickness Analysis of The Macula of Symptomatic and Asymptomatic Carriers of G11778A Mutations with Leber's Hereditary Optic NeuropathyDOI 10.21203/rs.3.rs-1454379/v1
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