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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Bibliografiska uppgifter
I publikationen:Invest Ophthalmol Vis Sci
Huvudupphovsmän: 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
Materialtyp: Artigo
Språk:Inglês
Publicerad: The Association for Research in Vision and Ophthalmology 2016
Ämnen:
Retina
Länkar: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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