CRISPR/Cas9 technology was used to generate a 23-bp deletion in the promoter of the tyrosinase gene, extending from position -107 through -85 with respect to the translation-initiating ATG codon. (J:94077)
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CRISPR/Cas9 technology was used to generate a 23-bp deletion in the promoter of the tyrosinase gene, extending from position -107 through -85 with respect to the translation-initiating ATG codon. (J:94077)