Genetic variation in the HTR1A gene and sudden infant death syndrome

Am J Med Genet A. 2008 Apr 1;146A(7):930-3. doi: 10.1002/ajmg.a.32112.
No abstract available

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Base Sequence
  • Case-Control Studies
  • DNA Primers
  • Female
  • Genetic Variation*
  • Humans
  • Infant
  • Male
  • Receptor, Serotonin, 5-HT1A / genetics*
  • Sudden Infant Death / genetics*

Substances

  • DNA Primers
  • Receptor, Serotonin, 5-HT1A