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@milk_cokie 基因编辑的做法是编辑腺病毒基因,然后让它感染人体。现在已经有一些遗传病可以治疗了,比如这个:https://t.co/ACiMIBEweR 治疗视网膜的遗传病。
@milk_cokie 基因编辑的做法是编辑腺病毒基因,然后让它感染人体。现在已经有一些遗传病可以治疗了,比如这个:https://t.co/ACiMIBEweR 治疗视网膜的遗传病。
Use of AAV Vectors for CRISPR-Mediated In Vivo Genome Editing in the Retina. https://t.co/4fGY6WwUs4
[PROTOCOL] Use of AAV Vectors for #CRISPR-Mediated In Vivo Genome Editing in the Retina. Yu W, Wu Z. In: Castle M. (eds) Adeno-Associated Virus Vectors. Methods in Molecular Biology 2019-02-20. https://t.co/vW15IOIYsl
Use of AAV Vectors for CRISPR-Mediated In Vivo Genome Editing in the Retina. https://t.co/jxMpEWREmb https://t.co/ylBAtdv686