Complete form of pachydermoperiostosis with SLCO2A1 gene mutation in a Korean family

J Dermatol. 2015 Jun;42(6):655-7. doi: 10.1111/1346-8138.12856. Epub 2015 Mar 21.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Humans
  • Male
  • Mutation
  • Organic Anion Transporters / genetics*
  • Osteoarthropathy, Primary Hypertrophic / genetics*
  • Republic of Korea
  • Siblings
  • Young Adult

Substances

  • Organic Anion Transporters
  • SLCO2A1 protein, human