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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
4 Suppl
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pubmed:dateCreated |
2009-4-6
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pubmed:abstractText |
To identify genes that are associated with premature ovarian failure, a linkage disequilibrium-based genome-wide association study with dense single nucleotide polymorphisms as genetic markers was performed. The acyl-coenzyme A synthetase long-chain family member 6 (ACSL6) gene on chromosome 5q31 was associated with premature ovarian failure and identified disease-susceptibility haplotypes.
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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:month |
Apr
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pubmed:issn |
1556-5653
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pubmed:author |
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pubmed:issnType |
Electronic
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pubmed:volume |
91
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1339-43
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pubmed:dateRevised |
2010-11-18
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pubmed:meshHeading |
pubmed-meshheading:18555221-Case-Control Studies,
pubmed-meshheading:18555221-Chromosomes, Human, Pair 5,
pubmed-meshheading:18555221-Coenzyme A Ligases,
pubmed-meshheading:18555221-Female,
pubmed-meshheading:18555221-Genetic Predisposition to Disease,
pubmed-meshheading:18555221-Haplotypes,
pubmed-meshheading:18555221-Humans,
pubmed-meshheading:18555221-Linkage Disequilibrium,
pubmed-meshheading:18555221-Polymorphism, Single Nucleotide,
pubmed-meshheading:18555221-Primary Ovarian Insufficiency
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pubmed:year |
2009
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pubmed:articleTitle |
Acyl-CoA synthetase long-chain family member 6 is associated with premature ovarian failure.
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pubmed:affiliation |
Medical Genomics Laboratory, Pochon CHA University, Gyeonggi-do, Korea.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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