CRISPR基因编辑叫板罕见免疫缺陷性疾病 (IMAGE)

American Association for the Advancement of Science (AAAS)

CRISPR基因编辑叫板罕见免疫缺陷性疾病

Caption

研究人员利用CRISPR-Cas9技术来纠正罹患某种罕见免疫缺陷性疾病患者血液干细胞中的基因突变；这些改造的细胞被成功地植入小鼠体内达5个月之久。

Credit

Chris Bickel / <i> Science Translational Medicine </i>(2017)

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