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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
1-2
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pubmed:dateCreated |
2008-6-19
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pubmed:abstractText |
This study investigated whether the catechol-O-methyltransferase (COMT) gene V158M single-nucleotide polymorphism (SNP) influences susceptibility to tardive dyskinesia (TD).
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:issn |
1423-0224
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pubmed:author |
pubmed-author:ChoiJung-EunJE,
pubmed-author:HanChangsuC,
pubmed-author:JoeSook-HaengSH,
pubmed-author:JungIn-KwaIK,
pubmed-author:KangSeung-GulSG,
pubmed-author:KimSeung-HyunSH,
pubmed-author:KimYong-KuYK,
pubmed-author:LeeHeon-JeongHJ,
pubmed-author:LeeMin-SooMS,
pubmed-author:OURY,
pubmed-author:ParkYoung-MinYM
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pubmed:copyrightInfo |
2008 S. Karger AG, Basel.
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pubmed:issnType |
Electronic
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pubmed:volume |
57
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
22-5
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pubmed:meshHeading |
pubmed-meshheading:18424907-Adult,
pubmed-meshheading:18424907-Asian Continental Ancestry Group,
pubmed-meshheading:18424907-Catechol O-Methyltransferase,
pubmed-meshheading:18424907-Dyskinesia, Drug-Induced,
pubmed-meshheading:18424907-Female,
pubmed-meshheading:18424907-Gene Expression,
pubmed-meshheading:18424907-Genome, Human,
pubmed-meshheading:18424907-Genotype,
pubmed-meshheading:18424907-Humans,
pubmed-meshheading:18424907-Male,
pubmed-meshheading:18424907-Polymorphism, Genetic,
pubmed-meshheading:18424907-Schizophrenia,
pubmed-meshheading:18424907-Severity of Illness Index
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pubmed:year |
2008
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pubmed:articleTitle |
Val158Met polymorphism in the catechol-O-methyltransferase (COMT) gene is not associated with tardive dyskinesia in schizophrenia.
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pubmed:affiliation |
Department of Psychiatry, Korea University College of Medicine, Seoul, South Korea.
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pubmed:publicationType |
Journal Article
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