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Intragenic deletions in 21 duchenne muscular dystrophy (DMD)/becker muscular dystrophy (BMD) families studied with the dystrophin DNA: location of breakpoints on hindill and bill exon-containing fragment maps, meiotic and mitotic origin of the mutations
Authors: Darras, Basil T. Blattner, Peggy Harper, John F. Spiro, Alfred J. Alter, Sheldon Francke, Uta
Citation: T. Darras, Basil et al., Intragenic deletions in 21 duchenne muscular dystrophy (DMD)/becker muscular dystrophy (BMD) families studied with the dystrophin DNA: location of breakpoints on hindill and bill exon-containing fragment maps, meiotic and mitotic origin of the mutations, American journal of human genetics , 43-II(5), 1988, pp. 620-629
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