A novel OSMR mutation in familial primary localized cutaneous amyloidosis in a Japanese family

J Dermatol Sci. 2009 Jul;55(1):64-5. doi: 10.1016/j.jdermsci.2009.03.003. Epub 2009 Apr 17.
No abstract available

Publication types

  • Letter

MeSH terms

  • Adult
  • Amyloidosis, Familial / genetics*
  • Amyloidosis, Familial / pathology
  • Female
  • Humans
  • Japan
  • Middle Aged
  • Mutation / genetics
  • Oncostatin M Receptor beta Subunit / genetics*
  • Pedigree
  • Skin Diseases / genetics*
  • Skin Diseases / pathology

Substances

  • OSMR protein, human
  • Oncostatin M Receptor beta Subunit