ReviewHuman gene therapy2023
CRISPR-Editing Therapy for Duchenne Muscular Dystrophy.
Francesco Chemello et al.PubMed ↗Full text ↗Publisher ↗
No numbers read from the abstract.
30 papers cite it
this papertrialcites it
ReviewHuman gene therapy2023
Francesco Chemello et al.PubMed ↗Full text ↗Publisher ↗
No numbers read from the abstract.