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Identification of point mutations in the dystrophin gene for accurate diagnosis of Duchenne and Becker Muscular Dystrophy

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.

Abstract

No abstract available

Item Type: Conference Item
URI: http://researchrepository.murdoch.edu.au/id/eprint/21919
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