Organic Solute Transporter Alpha Deficiency: A Disorder With Cholestasis, Liver Fibrosis, and Congenital Diarrhea

Hepatology. 2020 May;71(5):1879-1882. doi: 10.1002/hep.31087.
No abstract available

Publication types

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

MeSH terms

  • Child, Preschool
  • Cholestasis / genetics*
  • Diarrhea / congenital*
  • Humans
  • Liver / pathology*
  • Liver Cirrhosis / genetics*
  • Liver Cirrhosis / pathology
  • Male
  • Mutation
  • Pedigree
  • Receptors, G-Protein-Coupled / genetics*

Substances

  • Receptors, G-Protein-Coupled
  • SLC52A1 protein, human