ArticleMolecular therapy : the journal of the American Society of Gene Therapy2016

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

Benjamin Bakondi et al.PubMed ↗Full text ↗Publisher ↗

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