ReviewCells2022
CRISPR-Based Therapeutic Gene Editing for Duchenne Muscular Dystrophy: Advances, Challenges and Perspectives.
Guofang Chen et al.PubMed ↗Full text ↗Publisher ↗
No numbers read from the abstract.
20 papers cite it
this papercites it
ReviewCells2022
Guofang Chen et al.PubMed ↗Full text ↗Publisher ↗
No numbers read from the abstract.