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
Series:The Turkish Journal of Pediatrics
Online Access:https://turkjpediatr.org/article/view/2830
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