|
rdf:type |
|
|
lifeskim:mentions |
|
|
pubmed:issue |
23-24
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|
pubmed:dateCreated |
2010-10-11
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|
pubmed:abstractText |
We developed a CYP2D6 genotyping method that includes copy number variation (CNV) and recently known functional haplotypes using multiplex single-base extension (SBE).
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pubmed:language |
eng
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|
pubmed:journal |
|
|
pubmed:citationSubset |
IM
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|
pubmed:chemical |
|
|
pubmed:status |
MEDLINE
|
|
pubmed:month |
Dec
|
|
pubmed:issn |
1873-3492
|
|
pubmed:author |
|
|
pubmed:copyrightInfo |
Copyright © 2010 Elsevier B.V. All rights reserved.
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|
pubmed:issnType |
Electronic
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|
pubmed:day |
14
|
|
pubmed:volume |
411
|
|
pubmed:owner |
NLM
|
|
pubmed:authorsComplete |
Y
|
|
pubmed:pagination |
2043-8
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|
pubmed:meshHeading |
|
|
pubmed:year |
2010
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|
pubmed:articleTitle |
Robust CYP2D6 genotype assay including copy number variation using multiplex single-base extension for Asian populations.
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|
pubmed:affiliation |
Department of Clinical Pharmacology, Inje University Busan Paik Hospital, Busan, Republic of Korea.
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|
pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
|
