REPEATABILITY AND LONGITUDINAL ASSESSMENT OF FOVEAL CONE STRUCTURE IN CNGB3-ASSOCIATED ACHROMATOPSIA

PURPOSE: Congenital achromatopsia is an autosomal recessive disease causing substantial reduction or complete absence of cone function. Although believed to be a relatively stationary disorder, questions remain regarding the stability of cone structure over time. In this study, the authors sought to...

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Detalles Bibliográficos
Autores principales: Langlo, Christopher S., Erker, Laura R., Parker, Maria, Patterson, Emily J., Higgins, Brian P., Summerfelt, Phyllis, Razeen, Moataz M., Collison, Frederick T., Fishman, Gerald A., Kay, Christine N., Zhang, Jing, Weleber, Richard G., Yang, Paul, Pennesi, Mark E., Lam, Byron L., Chulay, Jeffrey D., Dubra, Alfredo, Hauswirth, William W., Wilson, David J., Carroll, Joseph
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Retina 2017
Materias:
Original Study
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5537050/
https://www.ncbi.nlm.nih.gov/pubmed/28145975
http://dx.doi.org/10.1097/IAE.0000000000001434

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5537050/
https://www.ncbi.nlm.nih.gov/pubmed/28145975
http://dx.doi.org/10.1097/IAE.0000000000001434

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