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 (Q24298532)
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(P31) (Q13442814)
(P304) 8466-74
(P407) (Q1860)
(P433) 25
(P478) 26
(P577) Tuesday, December 15, 1987
(P921) (Q3737532)
(Q14819285)
(Q785022)
(P1433) (Q764876)
(P1476) "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" (language: en)
(P2093) U T Meier
U A Meyer
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