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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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Pubblicato in:Invest Ophthalmol Vis Sci
Autori principali: 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
Natura: Artigo
Lingua:Inglês
Pubblicazione: The Association for Research in Vision and Ophthalmology 2016
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Accesso online: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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