Gee, P., Xu, H., & Hotta, A. Cellular Reprogramming, Genome Editing, and Alternative CRISPR Cas9 Technologies for Precise Gene Therapy of Duchenne Muscular Dystrophy. Wiley.
Chicago Style (17th ed.) CitationGee, Peter, Huaigeng Xu, and Akitsu Hotta. Cellular Reprogramming, Genome Editing, and Alternative CRISPR Cas9 Technologies for Precise Gene Therapy of Duchenne Muscular Dystrophy. Wiley.
MLA (9th ed.) CitationGee, Peter, et al. Cellular Reprogramming, Genome Editing, and Alternative CRISPR Cas9 Technologies for Precise Gene Therapy of Duchenne Muscular Dystrophy. Wiley.
Warning: These citations may not always be 100% accurate.