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The findings of optical coherence tomography of retinal degeneration in relation to the morphological and electroretinographic features in RPE65(−/−) mice
PURPOSE: Mutations of the gene encoding RPE65 cause Leber congenital amaurosis (LCA) retinitis pigmentosa (RP). The optical coherence tomography (OCT) is increasingly utilized to noninvasively evaluate various types of retinal diseases, including RP. The present study was conducted to characterize t...
Autores principales: | Tanabu, Reiko, Sato, Kota, Monai, Natsuki, Yamauchi, Kodai, Gonome, Takayuki, Xie, Yuting, Takahashi, Shizuka, Ishiguro, Sei-ichi, Nakazawa, Mitsuru |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6350961/ https://www.ncbi.nlm.nih.gov/pubmed/30695025 http://dx.doi.org/10.1371/journal.pone.0210439 |
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