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...

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Detalles Bibliográficos
Autores principales: Tanabu, Reiko, Sato, Kota, Monai, Natsuki, Yamauchi, Kodai, Gonome, Takayuki, Xie, Yuting, Takahashi, Shizuka, Ishiguro, Sei-ichi, Nakazawa, Mitsuru
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2019
Materias:
Research Article
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

Internet

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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