Long-term and age-dependent restoration of visual function in a mouse model of CNGB3-associated achromatopsia following gene therapy

Mutations in the CNGB3 gene account for >50% of all known cases of achromatopsia. Although of early onset, its stationary character and the potential for rapid assessment of restoration of retinal function following therapy renders achromatopsia a very attractive candidate for gene therapy. Here...

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Detalles Bibliográficos
Autores principales: Carvalho, Livia S., Xu, Jianhua, Pearson, Rachael A., Smith, Alexander J., Bainbridge, James W., Morris, Lynsie M., Fliesler, Steven J., Ding, Xi-Qin, Ali, Robin R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2011
Materias:
Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3140821/
https://www.ncbi.nlm.nih.gov/pubmed/21576125
http://dx.doi.org/10.1093/hmg/ddr218

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3140821/
https://www.ncbi.nlm.nih.gov/pubmed/21576125
http://dx.doi.org/10.1093/hmg/ddr218

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