v1
Customizable virus-like particles deliver CRISPR–Cas9 ribonucleoprotein for effective ocular neovascular and Huntington’s disease gene therapy
Identifier:nobleid.org/w1/20260418/28906863
Type:Journal Article
0 views
Embeddable Badge
[](https://nobleid.org/work/w1/20260418/28906863)
Bibliometric Analysis
Impact metrics, research fronts, co-authorship networks →