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Mapping of four translocation breakpoints within the Duchenne muscular dystrophy gene

โœ Scribed by Bodrug, S.E.; Burghes, A.H.M.; Ray, P.M.; Worton, R.G.

Book ID
123284029
Publisher
Elsevier Science
Year
1989
Tongue
English
Weight
790 KB
Volume
4
Category
Article
ISSN
0888-7543

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Mapping of X chromosome translocation breakpoints in females with Duchenne muscular dystrophy with respect to exons of the dystrophin gene
โœ D. J. Cockburn; E. A. Munro; I. W. Craig; Y. Boyd ๐Ÿ“‚ Article ๐Ÿ“… 1992 ๐Ÿ› Springer ๐ŸŒ English โš– 690 KB

There are rare female patients who suffer from Duchenne or Becker muscular dystrophy because they carry an X;autosome translocation with a breakpoint in the dystrophin gene. We have defined the positions of seven of these breakpoints with respect to exon-containing HindIII fragments detected by dyst