Macrosomia and neonatal hypoglycaemia in RW pedigree subjects with a mutation (Q268X) in the gene encoding hepatocyte nuclear factor 4alpha (HNF4A)

Diabetologia. 2007 Dec;50(12):2600-1. doi: 10.1007/s00125-007-0833-7. Epub 2007 Sep 22.
No abstract available

Publication types

  • Comment
  • Letter
  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Birth Weight / genetics
  • Codon, Nonsense*
  • Diabetes Mellitus, Type 1 / complications
  • Diabetes Mellitus, Type 1 / genetics
  • Female
  • Fetal Macrosomia / epidemiology
  • Fetal Macrosomia / genetics*
  • Hepatocyte Nuclear Factor 4 / genetics*
  • Humans
  • Hypoglycemia / congenital*
  • Hypoglycemia / epidemiology
  • Hypoglycemia / genetics*
  • Infant, Newborn
  • Male
  • Michigan
  • Pedigree*
  • Pregnancy
  • Prevalence
  • Retrospective Studies

Substances

  • Codon, Nonsense
  • HNF4A protein, human
  • Hepatocyte Nuclear Factor 4