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2. Identification of a new variant CYP2D6 allele with a single base deletion in exon 3 and its association with the poor metabolizer phenotype. Saxena R, Shaw GL, Relling MV, Frame JN, Moir DT, Evans WE, Caporaso N, Weiffenbach B. Hum Mol Genet; 1994 Jun; 3(6):923-6. PubMed ID: 7951238 [Abstract] [Full Text] [Related]