A new genetic defect in human CYP2C19: mutation of the initiation codon is responsible for poor metabolism of S-mephenytoin (Q28259441)

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A new genetic defect in human CYP2C19: mutation of the initiation codon is responsible for poor metabolism of S-mephenytoin
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    A new genetic defect in human CYP2C19: mutation of the initiation codon is responsible for poor metabolism of S-mephenytoin (English)
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    R J Ferguson
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    S M De Morais
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    S Benhamou
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    C Bouchardy
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    J Blaisdell
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    G Ibeanu
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    G R Wilkinson
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    T C Sarich
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    J M Wright
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    P Dayer
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    J A Goldstein
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    January 1998
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    284
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    1
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    356-61
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