TY  - GEN
AU  - Saxena,R
AU  - Shaw,G L
AU  - Relling,M V
AU  - Frame,J N
AU  - Moir,D T
AU  - Evans,W E
AU  - Caporaso,N
AU  - Weiffenbach,B
TI  - Identification of a new variant CYP2D6 allele with a single base deletion in exon 3 and its association with the poor metabolizer phenotype
SN  - 0964-6906
PY  - 1994///1130
KW  - Alleles
KW  - Base Sequence
KW  - Case-Control Studies
KW  - Cytochrome P-450 CYP2D6
KW  - Cytochrome P-450 Enzyme System
KW  - genetics
KW  - DNA
KW  - DNA Primers
KW  - Exons
KW  - Genetic Carrier Screening
KW  - Genetic Variation
KW  - Genotype
KW  - Humans
KW  - Lung Neoplasms
KW  - Mixed Function Oxygenases
KW  - Molecular Sequence Data
KW  - Phenotype
KW  - Polymerase Chain Reaction
KW  - Sequence Deletion
N1  - 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
UR  - https://doi.org/10.1093/hmg/3.6.923
ER  -