Analysis of deletions in DNA from patients with Becker and Duchenne muscular dystrophy.
Duchenne muscular dystrophy (DMD) is an X-linked recessive genetic disorder for which the biochemical defect is as yet unknown. Recently, two cloned segments of human X-chromosome DNA have been described which detect structural alterations within or near the genetic locus responsible for the disorde...
Principais autores: | , , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Journal article |
Idioma: | English |
Publicado em: |
1986
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