reference/23046991

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/23046991

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bibliographicCitation	Golbus JR, Stitziel NO, Zhao W, Xue C, Farrall M, McPherson R, Erdmann J, Deloukas P, Watkins H, Schunkert H, Samani NJ, Saleheen D, Kathiresan S, Reilly MP; CARDIoGRAMplusC4D, Myocardial Infarction Genetics (MIGen), Exome Sequencing Project and Early-Onset Myocardial Infarction (ESP EOMI), and the Pakistan Risk of Myocardial Infarction Study (PROMIS) Consortia*. Common and Rare Genetic Variation in CCR2, CCR5, or CX3CR1 and Risk of Atherosclerotic Coronary Heart Disease and Glucometabolic Traits. Circ Cardiovasc Genet. 2016 Jun;9(3):250–8. PMID: 27013693; PMCID: PMC5015681.
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date	201606
identifier	https://doi.org/10.1161/circgenetics.115.001374 https://pubmed.ncbi.nlm.nih.gov/PMC5015681 https://pubmed.ncbi.nlm.nih.gov/27013693
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language	English
source	https://pubmed.ncbi.nlm.nih.gov/ https://www.crossref.org/
title	Common and Rare Genetic Variation in CCR2 , CCR5 , or CX3CR1 and Risk of Atherosclerotic Coronary Heart Disease and Glucometabolic Traits
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