Sudden infant death syndrome: Case-control frequency differences in paired like homeobox (PHOX) 2B gene

Am J Med Genet A. 2006 Aug 1;140(15):1687-91. doi: 10.1002/ajmg.a.31336.
No abstract available

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alleles
  • Case-Control Studies
  • DNA / metabolism
  • Exons
  • Genotype
  • Homeodomain Proteins / genetics*
  • Humans
  • Infant
  • Introns
  • Mutation
  • Phenotype
  • Polymorphism, Genetic
  • Polymorphism, Single Nucleotide
  • Sudden Infant Death / genetics*
  • Transcription Factors / genetics*

Substances

  • Homeodomain Proteins
  • NBPhox protein
  • Transcription Factors
  • DNA