Li, Chao <br/><br/>
Novel HDAd/EBV Reprogramming Vector and Highly Efficient Ad/CRISPR-Cas Sickle Cell Disease Gene Correction.  [electronic resource] 

 -  Scientific reports  07 2016 
 - 30422 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>2045-2322 
<br/><br/><label>Standard No.: </label>10.1038/srep30422  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adenoviridae--metabolism<br/>Anemia, Sickle Cell--genetics<br/>Base Sequence<br/>CRISPR-Cas Systems--genetics<br/>Cell Line<br/>Genetic Therapy<br/>Genetic Vectors--metabolism<br/>Helper Viruses--metabolism<br/>Herpesvirus 4, Human<br/>Homozygote<br/>Humans<br/>Induced Pluripotent Stem Cells--metabolism