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

B. T. Darras, P. Blattner, J. F. Harper, A. J. Spiro, S. Alter, U. Francke

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Medicine & Life Sciences