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...

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Autori principali: Kunkel, L, Monaco, A, Bertelson, C, Colletti, C
Natura: Journal article
Lingua:English
Pubblicazione: 1986