A novel cDNA detects homozygous microdeletions in greater than 50% of type I spinal muscular atrophy patients

Terri G. Thompson, Christine J. Didonato, Louise R. Simard, Susan E. Ingraham, Arthur H.M. Burghes, Thomas O. Crawford, Camille Rochette, Jerry R. Mendell, John J. Wasmuth

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Biochemistry, Genetics and Molecular Biology

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