A mutation-independent CRISPR-Cas9–mediated gene targeting approach to treat a murine model of ornithine transcarbamylase deficiency
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Mingyao Li | H. Morizono | Lili Wang | James M. Wilson | Hongwei Yu | M. Batshaw | P. Bell | Jia Zhang | Zhenning He | Deirdre McMenamin | C. Breton | Yan Che | A. Saveliev | John White | Chenyu Xu | Yang Yang | Caitlin Latshaw | J. White | Peter Bell | Camilo Breton