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g Sickle-cell anemia arises from a mutation in the gene for the beta chain of human hemoglobin. The change from a GAG to a GTG in the mutant eliminates a cleavage site for the restriction enzyme MstII, which recognizes the target sequence CCTGAGG. These findings form the basis of a diagnostic test for
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g Sickle-cell anemia arises from a mutation in the gene for the beta chain of human hemoglobin. The...
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