SNX8: A candidate gene for 7p22 cardiac malformations including tetralogy of fallot

Am J Med Genet A. 2014 Feb;164A(2):554-6. doi: 10.1002/ajmg.a.36242. Epub 2013 Dec 5.
No abstract available

Publication types

  • Case Reports

MeSH terms

  • Child, Preschool
  • Chromosomes, Human, Pair 7*
  • Comparative Genomic Hybridization
  • Female
  • Heart Defects, Congenital / diagnosis
  • Heart Defects, Congenital / genetics*
  • Heart Defects, Congenital / therapy
  • Humans
  • Sorting Nexins / genetics*
  • Tetralogy of Fallot / diagnosis
  • Tetralogy of Fallot / genetics*
  • Tetralogy of Fallot / therapy

Substances

  • SNX8 protein, human
  • Sorting Nexins