In Vivo CRISPR/Cas9 Gene Editing Corrects Retinal Dystrophy in the S334ter-3 Rat Model of Autosomal Dominant Retinitis Pigmentosa

In Vivo CRISPR/Cas9 Gene Editing Corrects Retinal Dystrophy in the S334ter-3 Rat Model of Autosomal Dominant Retinitis Pigmentosa

Molecular Therapy 24,
556 (March 2016). doi:10.1038/mt.2015.220

Authors: Benjamin Bakondi, Wenjian Lv, Bin Lu, Melissa K Jones, Yuchun Tsai, Kevin J Kim, Rachelle Levy, Aslam Abbasi Akhtar, Joshua J Breunig, Clive N Svendsen & Shaomei Wang

Source: Molecular Therapy - March 8, 2016 Category: Genetics & Stem Cells Authors: Benjamin BakondiWenjian LvBin LuMelissa K JonesYuchun TsaiKevin J KimRachelle LevyAslam Abbasi AkhtarJoshua J BreunigClive N SvendsenShaomei Wang Source Type: research