Identification of a new variant CYP2D6 allele with a single base deletion in exon 3 and its association with the poor metabolizer phenotype-Reference-Cited by-同舟云学术

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Identification of a new variant CYP2D6 allele with a single base deletion in exon 3 and its association with the poor metabolizer phenotype

Published:1994 Issue:6 Volume:3 Page:923-926
ISSN:0964-6906
Container-title:Human Molecular Genetics
language:en
Short-container-title:Hum Mol Genet

Author:

Saxena Richa,Shaw Gall L.,Relling Mary V.,Frame James N.,Moir Donald T.,Evans William E.,Caporaso Neil,Weiffenbach Barbara

Publisher

Oxford University Press (OUP)

Subject

Genetics (clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/3/6/923/1608303/3-6-923.pdf

Cited by 104 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

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5. CYP2D6 genotype can help to predict effectiveness and safety during opioid treatment for chronic low back pain: results from a retrospective study in an Italian cohort;Pharmacogenomics and Personalized Medicine;2018-10

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