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Magnetic resonance imaging of children with Duchenne muscular dystrophy

โœ Scribed by A. Schreiber; W. L. Smith; V. Ionasescu; H. Zellweger; E. A. Franken; V. Dunn; J. Ehrhardt


Publisher
Springer-Verlag
Year
1987
Tongue
English
Weight
325 KB
Volume
17
Category
Article
ISSN
0301-0449

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The mdx mouse has a genetically homologous disease to Duchenne muscular dystrophy in humans. The disease progression, however, is not accompanied by the same level of fatty infiltration and muscle degeneration as occurs in humans. Thus, the presence of histological/ pathological changes in living md