APA

Saxena R., Shaw G. L., Relling M. V., Frame J. N., Moir D. T., Evans W. E., Caporaso N. & Weiffenbach B. (19941130). Identification of a new variant CYP2D6 allele with a single base deletion in exon 3 and its association with the poor metabolizer phenotype. : Human molecular genetics.

Chicago

Saxena R, Shaw G L, Relling M V, Frame J N, Moir D T, Evans W E, Caporaso N and Weiffenbach B. 19941130. Identification of a new variant CYP2D6 allele with a single base deletion in exon 3 and its association with the poor metabolizer phenotype. : Human molecular genetics.

Harvard

Saxena R., Shaw G. L., Relling M. V., Frame J. N., Moir D. T., Evans W. E., Caporaso N. and Weiffenbach B. (19941130). Identification of a new variant CYP2D6 allele with a single base deletion in exon 3 and its association with the poor metabolizer phenotype. : Human molecular genetics.

MLA

Saxena R, Shaw G L, Relling M V, Frame J N, Moir D T, Evans W E, Caporaso N and Weiffenbach B. Identification of a new variant CYP2D6 allele with a single base deletion in exon 3 and its association with the poor metabolizer phenotype. : Human molecular genetics. 19941130.