Estimation of the male and female mutation rates in Duchenne muscular dystrophy (DMD)
✍ Scribed by B. Müller; C. Dechant; G. Meng; S. Liechti-Gallati; R. A. Doherty; J. F. Hejtmancik; E. Bakker; A. P. Read; M. Jeanpierre; K. H. Fischbeck; G. Romeo; U. Francke; E. Wilichowski; C. R. Greenberg; C. Broeckhoven; C. Junien; C. R. Müller; T. Grimm
- Publisher
- Springer
- Year
- 1992
- Tongue
- English
- Weight
- 226 KB
- Volume
- 89
- Category
- Article
- ISSN
- 0340-6717
No coin nor oath required. For personal study only.
✦ Synopsis
We present the results of an international collaborative study aimed at estimating the ratio of male to female mutation rates in Duchenne muscular dystrophy based on the method of C. Müller and T. Grimm. With a sample size of 295, this ratio is found to be very close to 1, thus giving evidence for equal mutation rates in males and females in Duchenne muscular dystrophy.
📜 SIMILAR VOLUMES
Using blood cultures the response to gamma ()') radiation was examined in a male DMD and his mother, in a female DMD and her mother and in a normal control. In a series of experiments chromosome aberrations were determined after 3 separate )'-irradiation close levels: 0, 150, 300 rads. The DMD patie
The family of a male with Duchenne muscular dystrophy (DMD) and a deletion within the dystrophin gene has been studied. Polymerase chain reaction analysis of ectopic mRNA from peripheral blood T+B lymphocytes and the use of (CA) n repeat polymorphisms in and around the deleted region showed the prob