AAV as gene transfer vector has became a hot spot in gene therapy for eye diseases because of its safety,broad host range,low immunogenicity and long-term expression of therapeutic gene.

 
  • AAV作為基因轉移載體具有安全性好、宿主范圍廣、免疫原性低和攜帶的治療基因長(cháng)期表達等優(yōu)勢而成為眼病基因治療研究的熱點(diǎn)。
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