A novel frameshift mutation in the KIND1 gene in Turkish siblings with Kindler syndrome

N. Kaçar, N. Semerci, Ş Ergin, M. Pascucci, G. Zambruno, D. Castiglia

Research output: Contribution to journalArticlepeer-review

Original languageEnglish
Pages (from-to)1375-1377
Number of pages3
JournalBritish Journal of Dermatology
Issue number6
Publication statusPublished - Jun 2008


  • KIND1
  • Kindler syndrome
  • Mutation database
  • Poikiloderma

ASJC Scopus subject areas

  • Dermatology

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