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...
| Main Authors: | , , , |
|---|---|
| Format: | Journal article |
| Language: | English |
| Published: |
1986
|