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Failure to replicate an association of SNPs in the oxidized LDL receptor gene (OLR1) with CAD
BACKGROUND: The lectin-like oxidized LDL receptor LOX-1 (encoded by OLR1) is believed to play a key role in atherogenesis and some reports suggest an association of OLR1 polymorphisms with myocardial infarction (MI). We tested whether single nucleotide polymorphisms (SNPs) in OLR1 are associated wit...
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| Main Authors: | , , , , , , , , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2008
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2322963/ https://ncbi.nlm.nih.gov/pubmed/18384690 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2350-9-23 |
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