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Molecular genetic analysis in mild hyperhomocysteinemia: a common mutation in the methylenetetrahydrofolate reductase gene is a genetic risk factor for cardiovascular disease

Academic Article
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  • Overview
  • Identity
  • Additional Document Info
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Overview

authors

  • Kluijtmans, L. A. J.
  • van den Heuvel, L. P. W. J.
  • Boers, G. H. J.
  • Frosst, Phyllis
  • Stevens, E. M. B.
  • van Oost, B. A.
  • den Heijer, M.
  • Trijbels, F. J. M.
  • Rozen, R.
  • Blom, H. J.

publication date

  • January 1996

journal

  • American Journal of Human Genetics  Journal

subject areas

  • Alleles
  • Amino Acid Metabolism, Inborn Errors
  • Base Sequence
  • Cardiovascular Diseases
  • Confidence Intervals
  • Cystathionine beta-Synthase
  • DNA Primers
  • Genotype
  • Homocysteine
  • Humans
  • Methylenetetrahydrofolate Reductase (NADPH2)
  • Molecular Sequence Data
  • Oxidoreductases Acting on CH-NH Group Donors
  • Point Mutation
  • Polymerase Chain Reaction
  • Prevalence
  • Reference Values
  • Risk Factors
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Identity

PubMed Central ID

  • PMC1914961

International Standard Serial Number (ISSN)

  • 0002-9297

PubMed ID

  • 8554066
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Additional Document Info

start page

  • 35

end page

  • 41

volume

  • 58

issue

  • 1

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