Counsell, John R <br/><br/>
Lentiviral vectors can be used for full-length dystrophin gene therapy.  [electronic resource] 

 -  Scientific reports  03 2017 
 - 79 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>2045-2322 
<br/><br/><label>Standard No.: </label>10.1038/s41598-017-00152-5  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Cells, Cultured<br/>DNA Packaging<br/>Dystrophin--genetics<br/>Genetic Therapy<br/>Genetic Vectors--genetics<br/>HEK293 Cells<br/>HeLa Cells<br/>Humans<br/>Lentivirus--genetics<br/>Muscular Dystrophy, Duchenne--genetics<br/>Myoblasts, Skeletal--metabolism<br/>Recombination, Genetic<br/>Transduction, Genetic