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pubmed-article:1785656pubmed:abstractTextA new screening method involving the multiplex polymerase chain reaction was developed to detect dystrophin gene deletions in Japanese patients with Duchenne and Becker muscular dystrophy (DMD/BMD). Eleven exonic regions including deletion "hot spots" were analyzed. Gene deletions were found in 33% of 92 unrelated Japanese patients, mainly in the central portion (exons 43-52) and at the 5' end (exons 1-17). This is a useful laboratory test for the rapid genetic diagnosis of DMD/BMD.lld:pubmed
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pubmed-article:1785656pubmed:articleTitleA screening for dystrophin gene deletions in Japanese patients with Duchenne/Becker muscular dystrophy by the multiplex polymerase chain reaction.lld:pubmed
pubmed-article:1785656pubmed:affiliationDepartment of Clinical Genetics, Tokyo Metropolitan Institute of Medical Science, Japan.lld:pubmed
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