The induction effect of rifampicin on activity of mephenytoin 4′‐hydroxylase related to M1 mutation of CYP2C19 and gene dose
Author:
Affiliation:
1. Pharmacogenetics Research Institute, Hunan Medical University, Changsha, Hunan, P.R. China
Publisher
Wiley
Subject
Pharmacology (medical),Pharmacology
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1046/j.1365-2125.1998.00643.x
Reference16 articles.
1. Mephenytoin hydroxylation deficiency: Kinetics after repeated doses
2. Family studies of mephenytoin hydroxylation deficiency.;Inaba T;Am J Hum Gen,1986
3. S-mephenytoin 4-hydroxylase is inherited as an autosomal-recessive trait in Japanese families
4. The major genetic defect responsible for the polymorphism of S‐Mephenytoin metabolism in humans.;De Morais SMF;J Biol Chem,1994
5. Identification of a new genetic defect responsible for the polymorphism of S‐mephenytoin metabolism in Japanese.;De Morais SMF;Mol Pharmacol,1994
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