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Ethnic differentiation of copy number variation on chromosome 16p12.3 for association with obesity phenotypes in European and Chinese populations

OBJECTIVE: Genomic copy number variations (CNVs) have been strongly implicated as important genetic factors for obesity. A recent genome-wide association study identified a novel variant, rs12444979, which is in high linkage disequilibrium with CNV 16p12.3, for association with obesity in Europeans....

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Bibliografische gegevens
Hoofdauteurs: Yang, T-L, Guo, Y, Li, SM, Li, SK, Tian, Q, Liu, Y-J, Deng, H-W
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: 2012
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Online toegang:https://ncbi.nlm.nih.gov/pmc/articles/PMC3682477/
https://ncbi.nlm.nih.gov/pubmed/22391884
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/ijo.2012.31
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