Current status of pharmaceutical and genetic therapeutic approaches to treat DMD.
Duchenne muscular dystrophy (DMD) is a genetic disease affecting about one in every 3,500 boys. This X-linked pathology is due to the absence of dystrophin in muscle fibers. This lack of dystrophin leads to the progressive muscle degeneration that is often responsible for the death of the DMD patien...
| Główni autorzy: | , , , , , , , , , , |
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| Format: | Journal article |
| Język: | English |
| Wydane: |
2011
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