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Late-Onset Cone Photoreceptor Degeneration Induced by R172W Mutation in Rds and Partial Rescue by Gene Supplementation

PURPOSE: R172W is a common mutation in the human retinal degeneration slow (RDS) gene, associated with a late-onset dominant macular dystrophy. In this study, the authors characterized a mouse model that closely mimics the human phenotype and tested the feasibility of gene supplementation as a disea...

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Autores principales: Conley, Shannon, Nour, May, Fliesler, Steven J., Naash, Muna I.
Formato: Artigo
Lenguaje:Inglês
Publicado: 2007
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Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC2263142/
https://ncbi.nlm.nih.gov/pubmed/18055786
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1167/iovs.07-0663
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