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Detection of molecular deletions in the Chinese DMD patients using two amplified dystrophin sequences
1Shanghai Institute of Medical Genetics, Shanghai Children's Hospital, China.
Biochemical Medicine and Metabolic Biology
|April 1, 1992
Abstract:
This Brief Communication reports the detection of molecular deletions in Chinese DMD patients using two new amplified dystrophin DNAs involving the regions of exon 49 and 50. The results show that over 50% of the DMD deletions can be rapidly detected by PCR amplification of these two dystrophin sequences.