Kcnv2-KO 基因敲除小鼠

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3. Wissinger, Bernd, Schaich, Simone, Baumann, Britta, Zrenner, Eberhart, Kohl, Susanne. 2011. Large deletions of the KCNV2 gene are common in patients with cone dystrophy with supernormal rod response. In Human mutation, 32, 1398-406. doi:10.1002/humu.21580. https://pubmed.ncbi.nlm.nih.gov/21882291/

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