Solute carrier family 25 member 20 mutations may cause low-gamma-glutamyltransferase cholestasis without metabolic crisis in one Chinese infant

Acta Paediatr. 2020 Mar;109(3):623-624. doi: 10.1111/apa.15034. Epub 2019 Oct 14.
No abstract available

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Asian People
  • China
  • Cholestasis* / genetics
  • Humans
  • Infant
  • Membrane Transport Proteins / genetics*
  • Mutation
  • gamma-Glutamyltransferase*

Substances

  • Membrane Transport Proteins
  • SLC25A20 protein, human
  • gamma-Glutamyltransferase