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Single nucleotide polymorphisms in multiple novel thrombospondin genes may be associated with familial premature myocardial infarction

Academic Article
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  • Research
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Overview

authors

  • Topol, Eric
  • McCarthy, J.
  • Gabriel, S.
  • Moliterno, D. J.
  • Rogers, W. J.
  • Newby, L. K.
  • Freedman, M.
  • Metivier, J.
  • Cannata, R.
  • O'Donnell, C. J.
  • Kottke-Marchant, K.
  • Murugesan, G.
  • Plow, E. F.
  • Stenina, O.
  • Daley, G. Q.
  • GeneQuest Investigators, Collaborat

publication date

  • November 2001

journal

  • Circulation  Journal

subject areas

  • Adult
  • Age of Onset
  • Alleles
  • Case-Control Studies
  • Coronary Angiography
  • Coronary Artery Disease
  • Coronary Stenosis
  • Demography
  • Female
  • Genetic Predisposition to Disease
  • Genetic Testing
  • Genotype
  • Homozygote
  • Humans
  • Male
  • Methylenetetrahydrofolate Reductase (NADPH2)
  • Middle Aged
  • Myocardial Infarction
  • Odds Ratio
  • Oxidoreductases Acting on CH-NH Group Donors
  • Polymorphism, Single Nucleotide
  • Predictive Value of Tests
  • Thrombospondin 1
  • Thrombospondins
  • United States
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Research

keywords

  • atherosclerosis
  • coronary disease
  • genes
  • genetics
  • myocardial infarction
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Identity

International Standard Serial Number (ISSN)

  • 0009-7322

Digital Object Identifier (DOI)

  • 10.1161/hc4701.100910

PubMed ID

  • 11723011
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Additional Document Info

start page

  • 2641

end page

  • 2644

volume

  • 104

issue

  • 22

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