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Volumn 45, Issue 12, 1999, Pages 2273-2274

Frequencies of defective CYP2C19 alleles in a Hong Kong Chinese population: Detection of the rare allele CYP2C19*4

Author keywords

[No Author keywords available]

Indexed keywords

ANTICONVULSIVE AGENT; CYTOCHROME P450; PHENYTOIN;

EID: 0032737338     PISSN: 00099147     EISSN: None     Source Type: Journal    
DOI: 10.1093/clinchem/45.12.2273     Document Type: Article
Times cited : (26)

References (14)
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  • 8
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  • 9
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    • A new genetic defect in human CYP2C19: Mutation of the initiation codon is responsible for poor metabolism of S-mephenytoin
    • 9. Ferguson JF, de Morais SMF, Benhamou S, Bouchardy C, Blaisdell J, Ibeanu G, et al. A new genetic defect in human CYP2C19: mutation of the initiation codon is responsible for poor metabolism of S-mephenytoin. J Pharmacol Exp Ther 1998:284:356-61.
    • (1998) J Pharmacol Exp Ther , vol.284 , pp. 356-361
    • Ferguson, J.F.1    De Morais, S.M.F.2    Benhamou, S.3    Bouchardy, C.4    Blaisdell, J.5    Ibeanu, G.6
  • 10
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    • Identification of new human CYP2C19 alleles (CYP2C19*6 and CYP2C19*2B) in a Caucasian poor metabolizer of mephenytoin
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  • 11
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.