Intragenic deletions in 21 Duchenne muscular dystrophy (DMD)/Becker muscular dystrophy (BMD) families studied with the dystrophin cDNA: location of breakpoints on HindIII and BglII exon-containing fragment maps, meiotic and mitotic origin of the mutations

Following the strategy outlined in an accompanying paper, we studied 32 X-linked muscular dystrophy families (29 Duchenne [DMD] and three Becker [BMD] type) for abnormalities of HindIII and BglII fragments detected by the entire dystrophin cDNA. Twenty-one different single-intragenic deletions, and...

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Veröffentlicht in:American journal of human genetics 1988-11, Vol.43 (5), p.620-629
Hauptverfasser: DARRAS, B. T, BLATTNER, P, HARPER, J. F, SPIRO, A. J, ALTER, S, FRANCKE, U
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Sprache:eng
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