Residual Foveal Cone Structure in CNGB3-Associated Achromatopsia

PURPOSE: Congenital achromatopsia (ACHM) is an autosomal recessive disorder in which cone function is absent or severely reduced. Gene therapy in animal models of ACHM have shown restoration of cone function, though translation of these results to humans relies, in part, on the presence of viable co...

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Bibliografske podrobnosti
izdano v:Invest Ophthalmol Vis Sci
Main Authors: Langlo, Christopher S., Patterson, Emily J., Higgins, Brian P., Summerfelt, Phyllis, Razeen, Moataz M., Erker, Laura R., Parker, Maria, Collison, Frederick T., Fishman, Gerald A., Kay, Christine N., Zhang, Jing, Weleber, Richard G., Yang, Paul, Wilson, David J., Pennesi, Mark E., Lam, Byron L., Chiang, John, Chulay, Jeffrey D., Dubra, Alfredo, Hauswirth, William W., Carroll, Joseph
Format: Artigo
Jezik:Inglês
Izdano: The Association for Research in Vision and Ophthalmology 2016
Teme:
Retina
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC4978151/
https://ncbi.nlm.nih.gov/pubmed/27479814
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1167/iovs.16-19313
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