Human Genome Epidemiology Literature Finder
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Query Trace: Coronary Disease and SLC22A3[original query] |
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Two rare variants explain association with acute myocardial infarction in an extended genomic region including the apolipoprotein(A) gene. Annals of human genetics 2013 Jan 77 (1): 1. Koch W, Mueller JC, Schrempf M, Wolferstetter H, Kirchhofer J, Schömig A, Kastrati A |
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