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Molecular analysis of human muscular dystrophies

✍ Scribed by Dr. K. E. Davies; S. Forrest; T. Smith; S. Kenwrick; S. Ball; H. Dorkins; M. Patterson

Publisher
John Wiley and Sons
Year
1987
Tongue
English
Weight
719 KB
Volume
10
Category
Article
ISSN
0148-639X

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Duchenne muscular dystrophy (DMD) is a progressive and lethal neuromuscular disorder caused by a defective gene on the X chromosome. There is no effective treatment and the biochemical defect is yet unknown. Mapping of the DMD locus to band Xp21 in the short arm of the X chromosome has given rise to