Molecular genetics of Duchenne muscular dystrophy.
The use of random fragments of DNA from a defined region of the human X chromosome has led to the identification of a region of DNA that exhibits deletion in patients with DMD. The same region is tightly linked to the disorder in families segregating the disease. A systematic search of the region ha...
| Hauptverfasser: | , , , |
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| Format: | Journal article |
| Sprache: | English |
| Veröffentlicht: |
1986
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