最新科研成果
Gu X, Hu XD, Wang DQ, Xu ZJ, Wang F, Li D, Li GL, Yang H, Li HW*, Zuo EW*, Shu YL*(2022). Treatment of autosomal recessive hearing loss via in vivo CRISPR/Cas9-mediated optimized homology-directed repair in mice. Cell Res. doi:10.1038/s41422-022-00624-y