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- W2367802004 abstract "Objective To establish and evaluate methods suitable for Duchenne muscular dystrophy (DMD)gene diagnosis by multiplex polymerase chain reaction (mPCR)using ten pairs of primers. Methods Genomic DNA of 55 patients with DMD was extracted and subjected to mPCR of the dystrophin genes by 10 pairs of primers. Results The optimized ten-primer-assembly of exons,reactive system and cycling condition of multiplex-PCR were important for the amplification with the clear bands of electrophoresis. Among the 55 patients with DMD,various exonic deletions were detected in 28 cases (50.9%).In twenty-five cases,the deletions were located in exon 45～53,and in three cases,the deletions were located in exons 12～19,The deletion of exon 50 ranked the first,that of exon 45,47,51 and 52 did the second,and that of exon 12 and 53 did the third. Conclusion DMD gene deletions are mainly distributed in two hot spots surrounding exons 45～53 and 12～19. This method is valuable for clinical diagnosis of DMD gene deletion." @default.
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- W2367802004 date "2010-01-01" @default.
- W2367802004 modified "2023-09-26" @default.
- W2367802004 title "Detect Gene Deletion in Duchenne Muscular Dystrophy by Multiplex-PCR using Ten Pairs of Primers" @default.
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