. . . . . "CYP2C" . . . . "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" . . . . "2018-04-05T10:17:11.353+02:00"^^ . . . . . .