[23] Genetic tests which identify the principal defects in CYP2C19 responsible for the polymorphism in mephenytoin metabolism
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Publisher
Elsevier
Reference12 articles.
1. Genetic polymorphism of S-mephenytoin hydroxylation
2. Biochemistry and molecular biology of the human CYP2C subfamily
3. Evidence That CYP2C19 is the Major (S)-Mephenytoin 4'-Hydroxylase in Humans
4. Isolation and Characterization of Human Liver Cytochrome P450 2C19: Correlation between 2C19 and S-Mephenytoin 4′-Hydroxylation
5. The major genetic defect responsible for the polymorphism of S-mephenytoin metabolism in humans.
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