Characteristic immunohistochemical and ultrastructural findings indicate that Kindler"s syndrome is an apoptotic skin disorder.

C M Lanschuetzer, Wolfgang Muss (Co-author), M Emberger, G Pohla-Gubo, Alfred Klausegger (Co-author), Johann Bauer (Co-author), Helmut Hintner* (Last author)

*Corresponding author for this work

Research output: Contribution to journalCase reportpeer-review

19 Citations (Web of Science)
Original languageEnglish
Pages (from-to)553-560
JournalJOURNAL OF CUTANEOUS PATHOLOGY
Volume30
Issue number9
Publication statusPublished - 2003

Keywords

  • HEREDITARY ACROKERATOTIC POIKILODERMA
  • DYSKERATOSIS-CONGENITA
  • EPIDERMOLYSIS-BULLOSA
  • WEARY-KINDLER
  • IMMUNOFLUORESCENCE
  • MUTATIONS
  • DISEASE
  • PORPHYRIAS
  • FAMILIES
  • FEATURES

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