Corticortophin releasing factor 2 receptor agonist treatment significantly slows disease progression in mdx mice
<p>Abstract</p> <p>Background</p> <p>Duchenne muscular dystrophy results from mutation of the dystrophin gene, causing skeletal and cardiac muscle loss of function. The mdx mouse model of Duchenne muscular dystrophy is widely utilized to evaluate the potential of therap...
Main Authors: | , , , , , , , , , , , , |
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Format: | Article |
Language: | English |
Published: |
BMC
2007-07-01
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Series: | BMC Medicine |
Online Access: | http://www.biomedcentral.com/1741-7015/5/18 |