The molecular analysis of 127 DMD/BMD patients showed that 73 of them (57%) had deletions in the dystrophin gene. Two different methods were used in this study: (a) hybridization of HindIII-digested genomic DNA with nine cDNA probes corresponding to the entire 14kb cDNA of the DMD gene; and (b) simu
β¦ LIBER β¦
Screening for minor changes in the distal part of the human dystrophin gene in Greek DMD/BMD patients
β Scribed by Skouteli, Helen N; Metaxotou, Catherine; Kekou, Kiriaki; Mavrou, Ariadni; Florentin, Lina; Youroukos, Sotiris; Zafiriou, Dimitrios I
- Book ID
- 110024761
- Publisher
- Nature Publishing Group
- Year
- 1999
- Tongue
- English
- Weight
- 310 KB
- Volume
- 7
- Category
- Article
- ISSN
- 1018-4813
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