Wasala, Nalinda B <br/><br/>
Genomic removal of a therapeutic mini-dystrophin gene from adult mice elicits a Duchenne muscular dystrophy-like phenotype.  [electronic resource] 

 -  Human molecular genetics  07 2016 
 - 2633-2644 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, N.I.H., Extramural; Research Support, U.S. Gov't, Non-P.H.S. 
<br/><br/><label>ISSN: </label>1460-2083 
<br/><br/><label>Standard No.: </label>10.1093/hmg/ddw123  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Animals<br/>Dystrophin--genetics<br/>Gene Expression<br/>Gene Transfer Techniques<br/>Genetic Therapy--methods<br/>Genetic Vectors<br/>Genomics<br/>Mice<br/>Mice, Inbred CBA<br/>Mice, Inbred mdx<br/>Mice, Transgenic<br/>Muscle, Skeletal--metabolism<br/>Muscular Dystrophy, Animal--genetics<br/>Muscular Dystrophy, Duchenne--genetics<br/>Myocardium--metabolism