Familial early-onset hyperuricemia and gout associated with a newly identified dysfunctional variant in urate transporter ABCG2

Arthritis Res Ther. 2019 Oct 28;21(1):219. doi: 10.1186/s13075-019-2007-7.
No abstract available

Publication types

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

MeSH terms

  • ATP Binding Cassette Transporter, Subfamily G, Member 2 / genetics*
  • Female
  • Genetic Variation / genetics*
  • Gout / diagnosis*
  • Gout / genetics*
  • Humans
  • Hyperuricemia / diagnosis*
  • Hyperuricemia / genetics*
  • Male
  • Neoplasm Proteins / genetics*
  • Pedigree

Substances

  • ABCG2 protein, human
  • ATP Binding Cassette Transporter, Subfamily G, Member 2
  • Neoplasm Proteins