3' UTR polymorphism of the serotonin transporter gene and sudden infant death syndrome: haplotype analysis

Am J Med Genet A. 2006 Jul 1;140(13):1453-7. doi: 10.1002/ajmg.a.31261.
No abstract available

Publication types

  • Comparative Study
  • Letter
  • Research Support, Non-U.S. Gov't

MeSH terms

  • 3' Untranslated Regions / genetics*
  • Black People / genetics
  • Case-Control Studies
  • DNA Mutational Analysis
  • Female
  • Gene Frequency
  • Genotype
  • Haplotypes*
  • Humans
  • Infant
  • Male
  • Polymorphism, Genetic / genetics*
  • Serotonin Plasma Membrane Transport Proteins / genetics*
  • Sudden Infant Death / ethnology
  • Sudden Infant Death / genetics*
  • Sudden Infant Death / pathology
  • Syndrome
  • White People / genetics

Substances

  • 3' Untranslated Regions
  • SLC6A4 protein, human
  • Serotonin Plasma Membrane Transport Proteins