Gene therapy is a permanent replacement of a defective gene, usually treating an inherited disorder and usually using a viral vector.
基因治疗通常是利用病毒载体永久性地替换缺陷基因来治疗遗传性疾病。
Objective:To construct a recombinant defective retroviral vector carrying hNT3 gene and a stable virus-producing packaging cell lines , and then to identify them.
构建并鉴定携带人NT - 3基因的逆转录病毒载体以及稳定的包装细胞系。
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