Identification of an oncostatin M receptor mutation associated with familial primary cutaneous amyloidosis

Br J Dermatol. 2009 Oct;161(4):944-7. doi: 10.1111/j.1365-2133.2009.09237.x. Epub 2009 May 21.
No abstract available

Publication types

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

MeSH terms

  • Amyloidosis, Familial / genetics*
  • Amyloidosis, Familial / pathology
  • Female
  • Humans
  • Mutation, Missense / genetics*
  • Oncostatin M Receptor beta Subunit / genetics*
  • Oncostatin M Receptor beta Subunit / metabolism
  • Pedigree

Substances

  • Oncostatin M Receptor beta Subunit