In Vivo CRISPR/Cas9 Gene Editing Corrects Retinal Dystrophy...

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Molecular Therapy 2015 / 12

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

Bakondi, Benjamin, Lv, Wenjian, Lu, Bin, Jones, Melissa K., Tsai, Yuchun, Kim, Kevin J., Levy, Rachelle, Akhtar, Aslam A., Breunig, Joshua J., Svendsen, Clive N., Wang, Shaomei
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Language:
english
Journal:
Molecular Therapy
DOI:
10.1038/mt.2015.220
Date:
December, 2015
File:
PDF, 3.00 MB
english, 2015
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