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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Vydáno v:Retina
Hlavní autoři: 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
Médium: Artigo
Jazyk:Inglês
Vydáno: Retina 2017
Témata:
Original Study
On-line přístup: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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