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Analysis of dystrophin in fast- and slow-twitch skeletal muscles from mdx and dy2J mice at different ages

✍ Scribed by Dr. J. E. Anderson; Dr. L. Kao; Dr. B. H. Bressler; Dr. E. Gruesnstein


Publisher
John Wiley and Sons
Year
1990
Tongue
English
Weight
538 KB
Volume
13
Category
Article
ISSN
0148-639X

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## Abstract The __mdx__ mouse is the most commonly used animal model for Duchenne muscular dystrophy (DMD), a disease caused by the absence of dystrophin. Although much has been done to elucidate the structure and function of dystrophin and the dystrophin‐associated glycoprotein complex (DGC), litt