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Identification of carriers of Duchenne muscular dystrophy: Value of molecular analysis

✍ Scribed by LeRoy, Bonnie S. ;Uhrhammer, Nancy A. ;Steere, Karyn J. ;Boehm, Corinne D. ;King, Richard A. ;Rich, Stephen S. ;Williams, Preston P. ;Smith, Stephen A. ;de Martinville, Bérengère ;Reynolds, James F.


Publisher
John Wiley and Sons
Year
1988
Tongue
English
Weight
835 KB
Volume
31
Category
Article
ISSN
0148-7299

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Molecular analysis of Duchenne and Becke
✍ Ronald G. Worton 📂 Article 📅 1987 🏛 John Wiley and Sons 🌐 English ⚖ 818 KB

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