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PMID: 1635838 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

The frequency of revertants in mdx mouse genetic models for Duchenne muscular dystrophy.

Pediatric research ·Vol. 32 ·No. 1 ·1992-07-00 ·Pages 128-31

Danko I, Chapman V, Wolff JA

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.

Related Genes
mdx
MeSH Terms
Animals Dystrophin/genetics,metabolism Fluorescent Antibody Technique Immunoblotting Mice Mice, Mutant Strains Models, Genetic Muscles/metabolism,pathology Muscular Dystrophy, Animal/genetics,metabolism,pathology Mutation Myocardium/metabolism
Chemicals
Dystrophin
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Danko I
Department of Pediatrics, Waisman Center, University of Wisconsin, Madison 53705.
Chapman V
Wolff J A
Article Info
Journal
Pediatric research
Abbr.
Pediatr Res
ISSN
0031-3998
Published
1992-07-00
Pages
128-31
Language
English
Region
United States
NLM ID
0100714
Subset
IM
Grants
NICHD NIH HHS · HD00352 · United States
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