Stenina, M A <br/><br/>
Hereditary muscular dystrophy in MDX mice as a homologous model for introduction of cell technologies in the treatment of progressive muscular dystrophies in humans.  [electronic resource] 

 -  Bulletin of experimental biology and medicine  Oct 2004 
 - 425-8 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>0007-4888 
<br/><br/><label>Standard No.: </label>10.1007/s10517-005-0060-5  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Animals<br/>Dystrophin--genetics<br/>Exons<br/>Humans<br/>Male<br/>Mice<br/>Mice, Inbred mdx<br/>Motor Activity<br/>Muscle, Skeletal--pathology<br/>Muscular Dystrophy, Animal--genetics<br/>Point Mutation