Genetic Polymorphism of Human Cytochrome P-450 (S)-Mephenytoin 4-Hydroxylase. Studies with Human Autoantibodies Suggest a Functionally Altered Cytochrome P-450 Isozyme as Cause of the Genetic Deficiency

U. Thomas Meier, Urs A. Meyer

Research output: Contribution to journal › Article › peer-review

48 Scopus citations

Fingerprint

Dive into the research topics of 'Genetic Polymorphism of Human Cytochrome P-450 (S)-Mephenytoin 4-Hydroxylase. Studies with Human Autoantibodies Suggest a Functionally Altered Cytochrome P-450 Isozyme as Cause of the Genetic Deficiency'. Together they form a unique fingerprint.

Medicine & Life Sciences

Chemical Compounds