Common mutant alleles of CYP2D6 causing the defect of CYP2D6 enzyme activity in a Japanese population
Author:
Publisher
Wiley
Subject
Pharmacology (medical),Pharmacology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1046/j.1365-2125.2003.01782.x/fullpdf
Reference7 articles.
1. Frequencies of CYP2D6 mutant alleles in a normal Japanese population and metabolic activity of dextromethorphan O-demethylation in different CYP2D6 genotypes;Kubota;Br J Clin Pharmacol,2000
2. Frequent occurrence of CYP2D6*10 duplication allele in a Japanese population;Mitsunaga;Mutat Res,2002
3. A new CYP2D6 allele with a nine base insertion in exon 9 in a Japanese population associated with poor metabolizer phenotype;Yokoi;Pharmacogenetics,1996
4. A new variant CYP2D6 allele (CYP2D6*21) with a single base insertion in exon 5 in a Japanese population associated with a poor metabolizer phenotype;Chida;Pharmacogenetics,1999
5. CYP2D6 phenotype-genotype relationships in African-Americans and Caucasians in Los Angeles;Leathart;Pharmacogenetics,1998
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