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X CHROMOSOME IN DUCHENNE MUSCULAR DYSTROPHY

✍ Scribed by Skinner, R; Emery, A.E.H; Spowart, G; Buckton, K.E


Book ID
122704599
Publisher
The Lancet
Year
1982
Tongue
English
Weight
137 KB
Volume
319
Category
Article
ISSN
0140-6736

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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