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Duchenne muscular dystrophy in a female with 45,X/46,XX chromosome constitution

✍ Scribed by Motoki Sano; Fumiko Saito; Kohtaro Yamamoto; Akira Tonomura; Hiroshi Tsukagoshi

Book ID
105387192
Publisher
Nature Publishing Group
Year
1987
Tongue
English
Weight
561 KB
Volume
32
Category
Article
ISSN
1435-232X

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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