A novel homozygous mutation in the SLCO2A1 gene is associated with severe primary hypertrophic osteoarthropathy phenotype in a Saudi patient

Int J Dermatol. 2015 Jun;54(6):e233-5. doi: 10.1111/ijd.12770. Epub 2015 Jan 20.
No abstract available

Publication types

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

MeSH terms

  • Homozygote*
  • Humans
  • Male
  • Mutation*
  • Organic Anion Transporters / genetics*
  • Osteoarthropathy, Primary Hypertrophic / genetics*
  • Phenotype
  • Saudi Arabia
  • Severity of Illness Index
  • Young Adult

Substances

  • Organic Anion Transporters
  • SLCO2A1 protein, human