AAV-Mediated Cone Rescue in a Naturally Occurring Mouse Model of CNGA3-Achromatopsia

Achromatopsia is a rare autosomal recessive disorder which shows color blindness, severely impaired visual acuity, and extreme sensitivity to bright light. Mutations in the alpha subunits of the cone cyclic nucleotide-gated channels (CNGA3) are responsible for about 1/4 of achromatopsia in the U.S....

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Detalles Bibliográficos
Autores principales: Pang, Ji-jing, Deng, Wen-Tao, Dai, Xufeng, Lei, Bo, Everhart, Drew, Umino, Yumiko, Li, Jie, Zhang, Keqing, Mao, Song, Boye, Sanford L., Liu, Li, Chiodo, Vince A., Liu, Xuan, Shi, Wei, Tao, Ye, Chang, Bo, Hauswirth, William W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3324465/
https://www.ncbi.nlm.nih.gov/pubmed/22509403
http://dx.doi.org/10.1371/journal.pone.0035250

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3324465/
https://www.ncbi.nlm.nih.gov/pubmed/22509403
http://dx.doi.org/10.1371/journal.pone.0035250

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