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Familial primary localized cutaneous amyloidosis with an oncostatin M receptor-β mutation, Pro694Leu.

AuthorsS Schreml, B H Weber, J Schröder, H Siegmund, J Schaller, T Vogt, M Landthaler, I Schönbuchner, C Röcken, P Babilas
JournalClinical and experimental dermatology (Clin Exp Dermatol) Vol. 38 Issue 8 Pg. 932-5 (Dec 2013) ISSN: 1365-2230 [Electronic] England
PMID23692662 (Publication Type: Case Reports, Letter)
Chemical References
  • Oncostatin M Receptor beta Subunit
Topics
  • Adult
  • Amino Acid Substitution
  • Amyloidosis, Familial (genetics, pathology)
  • DNA Mutational Analysis
  • Female
  • Humans
  • Mutation, Missense
  • Oncostatin M Receptor beta Subunit (genetics)

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