𝔖 Bobbio Scriptorium
✦   LIBER   ✦

A molecular survey of Israeli Duchenne and Becker muscular dystrophy patients

✍ Scribed by Legum, C.; Shomrat, R.; Glassner, M.; Shiloh, Y.

Book ID
123398082
Publisher
Elsevier Science
Year
1994
Tongue
English
Weight
515 KB
Volume
48
Category
Article
ISSN
0753-3322

No coin nor oath required. For personal study only.

πŸ“œ SIMILAR VOLUMES

Molecular analysis of Duchenne and Becke
Molecular analysis of Duchenne and Becker muscular dystrophy
✍ Ronald G. Worton πŸ“‚ Article πŸ“… 1987 πŸ› John Wiley and Sons 🌐 English βš– 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

Molecular genetic analysis of 67 patient
Molecular genetic analysis of 67 patients with duchenne/becker muscular dystrophy
✍ Susanne Niemann-Seyde; Ryszard Slomski; Frauke Rininsland; Ute Ellermeyer; Jolan πŸ“‚ Article πŸ“… 1992 πŸ› Springer 🌐 English βš– 723 KB

A total of 56 Duchenne muscular dystrophy (DMD) patients and 11 Becker muscular dystrophy (BMD) patients was analyzed by extended "multiplex" amplification of the DMD/BMD gene; deletions were found in 60% of these patients. The data obtained were used to test the frameshift hypothesis and to compare