1. Cellular Reprogramming, Genome Editing, and Alternative CRISPR Cas9 Technologies for Precise Gene Therapy of Duchenne Muscular Dystrophy. (15th May 2017) Authors: Gee, Peter; Xu, Huaigeng; Hotta, Akitsu Other Names: Suzuki Masatoshi Academic Editor. Journal: Stem cells international Issue: Volume 2017(2017) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗