ArticleMolecular therapy : the journal of the American Society of Gene Therapy2016

High Efficiency CRISPR/Cas9-mediated Gene Editing in Primary Human T-cells Using Mutant Adenoviral E4orf6/E1b55k "Helper" Proteins.

Kamila S Gwiazda et al.PubMed ↗Full text ↗Publisher ↗

No numbers read from the abstract.