Goldstein, J A <br/><br/>
Frequencies of the defective CYP2C19 alleles responsible for the mephenytoin poor metabolizer phenotype in various Oriental, Caucasian, Saudi Arabian and American black populations.  [electronic resource] 

 -  Pharmacogenetics  Feb 1997 
 - 59-64 p.  digital 
<br/><br/> Publication Type: Comparative Study; Journal Article 
<br/><br/><label>ISSN: </label>0960-314X 
<br/><br/><label>Standard No.: </label>10.1097/00008571-199702000-00008  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Alleles<br/>Arabs--genetics<br/>Aryl Hydrocarbon Hydroxylases<br/>Asian People--genetics<br/>Black People--genetics<br/>Confidence Intervals<br/>Cytochrome P-450 CYP2C19<br/>Cytochrome P-450 Enzyme System--genetics<br/>Gene Frequency<br/>Heterozygote<br/>Homozygote<br/>Humans<br/>Mephenytoin--metabolism<br/>Mixed Function Oxygenases--genetics<br/>Philippines<br/>Polymorphism, Genetic<br/>Saudi Arabia<br/>Taiwan<br/>White People<br/>Black or African American