Naturally-occurring myopia and loss of cone function in a sheep model of achromatopsia

Achromatopsia is an inherited retinal disease characterized by loss of cone photoreceptor function. Day blind CNGA3 mutant Improved Awassi sheep provide a large animal model for achromatopsia. This study measured refractive error and axial length parameters of the eye in this model and evaluated chr...

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Detalles Bibliográficos
Autores principales: Ross, Maya, Ofri, Ron, Aizenberg, Itzhak, Abu–Siam, Mazen, Pe’er, Oren, Arad, Dikla, Rosov, Alexander, Gootwine, Elisha, Dvir, Hay, Honig, Hen, Obolensky, Alexey, Averbukh, Edward, Banin, Eyal, Gantz, Liat
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7653946/
https://www.ncbi.nlm.nih.gov/pubmed/33168939
http://dx.doi.org/10.1038/s41598-020-76205-z

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