[Hereditary hypouricemia]

Nihon Jinzo Gakkai Shi. 2011;53(2):142-5.
[Article in Japanese]
No abstract available

Publication types

  • Review

MeSH terms

  • ATP Binding Cassette Transporter, Subfamily G, Member 2
  • ATP-Binding Cassette Transporters / genetics
  • Glucose Transport Proteins, Facilitative / genetics*
  • Humans
  • Monocarboxylic Acid Transporters / genetics
  • Mutation*
  • Neoplasm Proteins / genetics
  • Organic Anion Transporters / genetics*
  • Organic Cation Transport Proteins / genetics*
  • Renal Tubular Transport, Inborn Errors / diagnosis
  • Renal Tubular Transport, Inborn Errors / epidemiology
  • Renal Tubular Transport, Inborn Errors / genetics
  • Renal Tubular Transport, Inborn Errors / physiopathology
  • Urinary Calculi / diagnosis
  • Urinary Calculi / epidemiology
  • Urinary Calculi / genetics
  • Urinary Calculi / physiopathology

Substances

  • ABCG2 protein, human
  • ATP Binding Cassette Transporter, Subfamily G, Member 2
  • ATP-Binding Cassette Transporters
  • Glucose Transport Proteins, Facilitative
  • Monocarboxylic Acid Transporters
  • Neoplasm Proteins
  • Organic Anion Transporters
  • Organic Cation Transport Proteins
  • SLC16A9 protein, human
  • SLC22A12 protein, human
  • SLC2A9 protein, human

Supplementary concepts

  • Renal hypouricemia