Information Journal Paper
APA:
CopyGOLDSTEIN, J.A., ISHIZAKI, T., CHIBA, K., DE MORAIS, S.M., BELL, D., & KRAHN, P.M.. (1997). FREQUENCIES OF THE DEFECTIVE CYP2C19 ALLELES RESPONSIBLE FOR THE MEPHENYTOIN POOR METABOLIZER PHENOTYPE IN VARIOUS ORIENTAL, CAUCASIAN, SAUDI ARABIAN AND AMERICAN BLACK POPULATIONS. PHARMACOGENETICS AND GENOMICS, 7(-), 59-64. SID. https://sid.ir/paper/541155/en
Vancouver:
CopyGOLDSTEIN J.A., ISHIZAKI T., CHIBA K., DE MORAIS S.M., BELL D., KRAHN P.M.. FREQUENCIES OF THE DEFECTIVE CYP2C19 ALLELES RESPONSIBLE FOR THE MEPHENYTOIN POOR METABOLIZER PHENOTYPE IN VARIOUS ORIENTAL, CAUCASIAN, SAUDI ARABIAN AND AMERICAN BLACK POPULATIONS. PHARMACOGENETICS AND GENOMICS[Internet]. 1997;7(-):59-64. Available from: https://sid.ir/paper/541155/en
IEEE:
CopyJ.A. GOLDSTEIN, T. ISHIZAKI, K. CHIBA, S.M. DE MORAIS, D. BELL, and P.M. KRAHN, “FREQUENCIES OF THE DEFECTIVE CYP2C19 ALLELES RESPONSIBLE FOR THE MEPHENYTOIN POOR METABOLIZER PHENOTYPE IN VARIOUS ORIENTAL, CAUCASIAN, SAUDI ARABIAN AND AMERICAN BLACK POPULATIONS,” PHARMACOGENETICS AND GENOMICS, vol. 7, no. -, pp. 59–64, 1997, [Online]. Available: https://sid.ir/paper/541155/en