Heterozygous FIC1 deficiency: a new genetic predisposition to transient neonatal cholestasis

J Pediatr Gastroenterol Nutr. 2010 Apr;50(4):447-9. doi: 10.1097/MPG.0b013e3181cd2725.
No abstract available

Publication types

  • Case Reports

MeSH terms

  • Adenosine Triphosphatases / genetics*
  • Cholestasis / genetics*
  • Genetic Predisposition to Disease*
  • Heterozygote
  • Humans
  • Infant
  • Infant, Newborn
  • Male
  • Sequence Deletion*

Substances

  • Adenosine Triphosphatases
  • ATP8B1 protein, human