A new genetic defect in human CYP2C19: mutation of the initiation codon is responsible for poor metabolism of S-mephenytoin.

Autor: J, Ferguson R, M, De Morais S, S, Benhamou, C, Bouchardy, J, Blaisdell, G, Ibeanu, R, Wilkinson G, C, Sarich T, M, Wright J, P, Dayer, A, Goldstein J

Publikováno v: The Journal of Pharmacology and Experimental Therapeutics; January 1998, Vol. 284 Issue: 1 p356-61, 6p