Identification of point mutations in the dystrophin gene for accurate diagnosis of Duchenne and Becker Muscular Dystrophy
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Wilton, S.D. and Laing, N.G. (1993) Identification of point mutations in the dystrophin gene for accurate diagnosis of Duchenne and Becker Muscular Dystrophy. In: International Conference on Clinical Molecular Biology.
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| Item Type: | Conference Item |
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| URI: | http://researchrepository.murdoch.edu.au/id/eprint/21919 |
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