Investigation of Structural Alterations in Inherited Retinal Diseases: A Quantitative SD-OCT-Analysis of Retinal Layer Thicknesses in Light of Underlying Genetic Mutations

Inherited retinal diseases can result from various genetic defects and are one of the leading causes for blindness in the working-age population. The present study aims to provide a comprehensive description of changes in retinal structure associated with phenotypic disease entities and underlying g...

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Detalles Bibliográficos
Autores principales: Gersch, Julia, Hufendiek, Katerina, Delarocque, Julien, Framme, Carsten, Jacobsen, Christina, Stöhr, Heidi, Kellner, Ulrich, Hufendiek, Karsten
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9788460/
https://www.ncbi.nlm.nih.gov/pubmed/36555650
http://dx.doi.org/10.3390/ijms232416007

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9788460/
https://www.ncbi.nlm.nih.gov/pubmed/36555650
http://dx.doi.org/10.3390/ijms232416007

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