Congenital diaphragmatic abnormalities in arterial tortuosity syndrome patients who carry mutations in the SLC2A10 gene

Clin Genet. 2009 Jun;75(6):588-9. doi: 10.1111/j.1399-0004.2009.01165.x.
No abstract available

Publication types

  • Kommentar
  • Letter

MeSH terms

  • Arteries / abnormalities*
  • Cardiovascular Diseases / complications*
  • Cardiovascular Diseases / congenital
  • Cardiovascular Diseases / genetics*
  • Glucose Transport Proteins, Facilitative / genetics*
  • Hernia, Diaphragmatic / complications
  • Hernias, Diaphragmatic, Congenital*
  • Humans
  • Mutation*
  • Syndrome

Substances

  • Glucose Transport Proteins, Facilitative
  • SLC2A10 protein, human