We studied 160 cases of Duchenne muscular dystrophy (DMD) drawn from all parts of India, using multiplex PCR of 27 exons. Of these, 103 (64.4%) showed intragenic deletions. Most (69.7%) of the deletions involved exons 45-51. The phenotype of cases with deletion of single exons did not differ signifi
The candidate gene approach in alcoholism: are there gender-specific differences?
β Scribed by N. Wodarz; G. Bobbe; P. Eichhammer; H. G. Weijers; G. A. Wiesbeck; M. Johann
- Publisher
- Springer Vienna
- Year
- 2003
- Tongue
- English
- Weight
- 164 KB
- Volume
- 6
- Category
- Article
- ISSN
- 1434-1816
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