Deletion analysis and clinical correlations in patients with Xp21 linked muscular dystrophy
We carried out molecular deletion analysis on 142 patients with Duchenne/Becker muscular dystrophy which covered 25 exons of the dystrophin gene. We also evaluated the results by comparing with the clinical findings and examples in the literature. A deletion ratio of 63.7% was achieved. Exon...
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| Main Authors: | Ayfer Ulgenalp, Ferda Ozkinay, Eray Dirik, Sarenur Tütüncüoğlu, Gülşen Dizdarer, Nedret Uran, Hatice Karasoy, Gül Sağin-Saylam, Semra Kurul, Tülin Hizli, Elçin Bora, Ozlem Giray, Derya Erçal |
|---|---|
| Format: | Article |
| Language: | English |
| Published: |
Hacettepe University Institute of Child Health
2004-10-01
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| Series: | The Turkish Journal of Pediatrics |
| Online Access: | https://turkjpediatr.org/article/view/2830 |
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