"Goldin" : a triton-insoluble protein specifically upregulated in MDX skeletal muscle
Human Duchenne Muscular Dystrophy (DMD) is an X-linked recessive disorder with progressive muscle degeneration leading to death in the second decade of life. The pathogenesis of this disorder and its genetic correlate in the mutant mdx mouse, have been linked to the absence of dystrophin (Hoffman...
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| Format: | Others |
| Language: | English |
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2009
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| Online Access: | http://hdl.handle.net/2429/4456 |