The time course of changes in skeletal muscle metabolites during muscle repair, as detected by proton nuclear magnetic resonance spectroscopy
Duchenne muscular dystrophy (DMD) is characterized by progressive deterioration of muscles due to the lack of dystrophin. To date there is no effective method for monitoring DMD progression without reverting to biopsies and subjective muscle strength testing. With the discovery of the mdx mouse mus...
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| Language: | en_US |
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2007
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| Online Access: | http://hdl.handle.net/1993/2105 |