Saxena, R <br/><br/>
Identification of a new variant CYP2D6 allele with a single base deletion in exon 3 and its association with the poor metabolizer phenotype.  [electronic resource] 

 -  Human molecular genetics  Jun 1994 
 - 923-6 p.  digital 
<br/><br/> Publication Type: Clinical Trial; Comparative Study; Controlled Clinical Trial; Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S. 
<br/><br/><label>ISSN: </label>0964-6906 
<br/><br/><label>Standard No.: </label>10.1093/hmg/3.6.923  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Alleles<br/>Base Sequence<br/>Case-Control Studies<br/>Cytochrome P-450 CYP2D6<br/>Cytochrome P-450 Enzyme System--genetics<br/>DNA--genetics<br/>DNA Primers<br/>Exons<br/>Genetic Carrier Screening<br/>Genetic Variation<br/>Genotype<br/>Humans<br/>Lung Neoplasms--genetics<br/>Mixed Function Oxygenases--genetics<br/>Molecular Sequence Data<br/>Phenotype<br/>Polymerase Chain Reaction<br/>Sequence Deletion