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 biology of duchenne and Becker's muscular dystrophy: Clinical applications
โ Scribed by David H. Gutmann; Kenneth H. Fischbeck
- Publisher
- John Wiley and Sons
- Year
- 1989
- Tongue
- English
- Weight
- 646 KB
- Volume
- 26
- Category
- Article
- ISSN
- 0364-5134
No coin nor oath required. For personal study only.
โฆ Synopsis
Recent advances in molecular genetics have led to the isolation of the gene defective in patients with Duchenne and Becker's muscular dystrophy and the characterization of its protein product, dystrophin. In this communication, the developments culminating in the identification of the Duchenne muscular dystrophy locus are reviewed. The practical applications of this research and pitfalls that limit prenatal diagnosis and carrier detection are discussed.
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We think that the article by contains inaccurate and misleading information. The first important criticism is the title, which implies that longitudinal data on the clinical course of the disease are to be presented. This can only be measured by observation over a period of time, and no such data w