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December 15, 2015Molecular TherapyOpen Access

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

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BBBenjamin BakondiWLWenjian LvBLBin Lü

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Bakondi et al. (2015) studied this question.

synapsesocial.com/papers/6a991fdaaa63da60ef78d25ehttps://doi.org/10.1038/mt.2015.220
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