CYP450 Genotype-Phenotype Concordance Using the Geneva Micrococktail in a Clinical Setting
Pharmacokinetic variability is a major source of differences in drug response and can be due to genetic variants and/or drug-drug interactions. Cytochromes P450 are among the most studied enzymes from a pharmacokinetic point of view. Their activity can be measured by phenotyping, and/or predicted by...
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Main Authors: | , , , , , , |
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Frontiers Media S.A.,
2021-08-01T00:00:00Z.
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