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Advanced filters: Author: Jing-Tong Luo Clear advanced filters

  • Genetic muscle diseases are difficult to treat due to challenges in delivering gene editors to muscles throughout the body. Here, authors engineer muscle-specific virus-like particles that fuse with skeletal muscle cells to deliver CRISPR tools and restore dystrophin in a DMD model.

    • Shi-Kun Zhou
    • Jing-Tong Luo
    • Jun Wang
    ResearchOpen Access
    Nature Communications
    Volume: 16, P: 1-12