Heterozygous prothrombin G20210A gene mutation in a patient with livedoid vasculitis

Arch Dermatol. 2003 Aug;139(8):1081-3. doi: 10.1001/archderm.139.8.1081-b.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Adult
  • Female
  • Heterozygote*
  • Humans
  • Mutation / genetics*
  • Prothrombin / genetics*
  • Skin Diseases, Vascular / genetics*
  • Skin Diseases, Vascular / pathology
  • Skin Diseases, Vascular / therapy
  • Vasculitis / genetics*
  • Vasculitis / pathology
  • Vasculitis / therapy

Substances

  • Prothrombin