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Transporters genotype analysis

ITABLE 14.1. Some polymorphically expressed metabolic enzymes and transporters that may be amenable to genotype analysis for individualization of drug regimens... [Pg.384]

Wang, Y., et al. Functional analysis of mutations in the OCTN2 transporter causing primary carnitine deficiency lack of genotype-phenotype correlation. Hum. Mutat. 2000, 16, 401-407. [Pg.278]


See other pages where Transporters genotype analysis is mentioned: [Pg.50]    [Pg.325]    [Pg.508]    [Pg.95]    [Pg.272]    [Pg.342]    [Pg.462]    [Pg.266]    [Pg.1095]    [Pg.202]    [Pg.3259]    [Pg.77]    [Pg.101]    [Pg.508]    [Pg.577]    [Pg.606]    [Pg.540]    [Pg.285]    [Pg.382]    [Pg.307]    [Pg.291]    [Pg.589]    [Pg.382]    [Pg.216]    [Pg.387]   
See also in sourсe #XX -- [ Pg.384 ]




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