Complementary DNA Probes for the Duchenne Muscular Dystrophy Locus Demonstrate a Previously Undetectable Deletion in a Patient With Dystrophic Myopathy, Glycerol Kinase Deficiency, and Congenital Adrenal Hypoplasia.

Journal of Clinical Investigation - United States
doi 10.1172/jci113890
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American Society for Clinical Investigation

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