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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Bibliografske podrobnosti
izdano v:Retina
Main Authors: 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
Format: Artigo
Jezik:Inglês
Izdano: Retina 2017
Teme:
Original Study
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC5537050/
https://ncbi.nlm.nih.gov/pubmed/28145975
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1097/IAE.0000000000001434
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