使用CRISPR / Cas9进行基因重组编辑 (IMAGE) Universidad Carlos III de Madrid Caption 研究人员使用CRISPR / Cas9工具对基因进行重组编辑。该工具可准确、安全地去除来自患者皮肤干细胞致 病突变基因COL7A1外显子80,使重新编辑的细胞产生胶原蛋白7的功能变体 Credit UC3M Usage Restrictions None License Licensed content Disclaimer: AAAS and EurekAlert! are not responsible for the accuracy of news releases posted to EurekAlert! by contributing institutions or for the use of any information through the EurekAlert system.