| Literature DB >> 1635838 |
I Danko1, V Chapman, J A Wolff.
Abstract
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.Entities:
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Year: 1992 PMID: 1635838 DOI: 10.1203/00006450-199207000-00025
Source DB: PubMed Journal: Pediatr Res ISSN: 0031-3998 Impact factor: 3.756