Lentiviral vectors in hematopoietic stem cell therapies: mainstay technology, or simply a bridge to gene editing?

Lentiviral vectors in hematopoietic stem cell therapies: mainstay technology, or simply a bridge to gene editing?
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造血干细胞疗法中的慢病毒载体:主流技术,还是基因编辑的桥梁?

DOI:
10.18609/cgti.2018.092
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发表时间:
2018
期刊:
Cell and Gene Therapy Insights
影响因子:
--
通讯作者:
Moore M
Moore M
中科院分区:
--
文献类型:
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作者:
Moore M

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