ABCG2 rs2231142 variant in hyperuricemia is modified by SLC2A9 and SLC22A12 polymorphisms and cardiovascular risk factors in an elderly community-dwelling population

BACKGROUND: The ABCG2 rs2231142 single nucleotide polymorphism (SNP) is one of the most significant genetic variants associated with hyperuricemia (HUA) in Asian populations. However, the risk of ABCG2 rs2231142 variants for HUA could interact with other important HUA risk variants and cardiovascula...

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Vydáno v:BMC Med Genet
Hlavní autoři: Liu, Jia, Yang, Wei, Li, Yun, Wei, Zhanyun, Dan, Xiaojuan
Médium: Artigo
Jazyk:Inglês
Vydáno: BioMed Central 2020
Témata:
Research Article
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC7077001/
https://ncbi.nlm.nih.gov/pubmed/32183743
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12881-020-0987-4
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