Distinct phenotypes and genotypes of debrisoquine hydroxylation among Europeans and Chinese [letter]
Author:
Publisher
Wiley
Subject
Pharmacology (medical),Pharmacology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2125.1991.tb05629.x/fullpdf
Reference6 articles.
1. Debrisoquine phenotype and genotype in Chinese;Caporaso;Lancet,1989
2. A family and population study of the genetic polymorphism of debrisoquine oxidation in a white British population;Evans;J. med. Genet.,1980
3. Low frequency of slow debrisoquine hydroxylation in a native Chinese population;Lou;Lancet,1989
4. Interethnic differences in genetic polymorphism of debrisoquine and mephenytoin hydroxylation between Japanese and Caucasian populations;Nakamura;Clin. Pharmac. Ther.,1987
5. Two mutant alleles of the human cytochrome P-450 db1 gene (P450C2D1) associated with genetically deficient metabolism of debrisoquine and other drugs;Skoda;Proc. Natl. Acad. Sci. USA,1988
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