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| http://purl.uniprot.org/citations/1635838 | http://www.w3.org/2000/01/rdf-schema#comment | "The mdx mouse has been used for the development of cellular and gene therapies for Duchenne muscular dystrophy. The relatively frequent occurrence of dystrophin-positive muscle cells called revertants has hampered these efforts by interfering with data interpretation. The mdx4cv and mdx5cv dystrophin mouse mutants have approximately 10-fold fewer revertants than the mdx mutant at both 2 and 6 mo. The mdx3cv dystrophin mouse mutant may be a useful model for some types of human dystrophin deficiencies in which the levels of dystrophin are low but not completely absent."xsd:string |
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| http://purl.uniprot.org/citations/1635838 | http://purl.uniprot.org/core/author | "Chapman V."xsd:string |
| http://purl.uniprot.org/citations/1635838 | http://purl.uniprot.org/core/author | "Wolff J.A."xsd:string |
| http://purl.uniprot.org/citations/1635838 | http://purl.uniprot.org/core/author | "Danko I."xsd:string |
| http://purl.uniprot.org/citations/1635838 | http://purl.uniprot.org/core/date | "1992"xsd:gYear |
| http://purl.uniprot.org/citations/1635838 | http://purl.uniprot.org/core/name | "Pediatr Res"xsd:string |
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| http://purl.uniprot.org/citations/1635838 | http://purl.uniprot.org/core/title | "The frequency of revertants in mdx mouse genetic models for Duchenne muscular dystrophy."xsd:string |
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