Complete homozygous deletion of CTSC in an Iranian family with Papillon-Lefèvre syndrome

Research output: Contribution to journal › Case report › Contributed › peer-review

Contributors

  • Hans K Schackert - , Department of Surgical Research (Author)
  • Farzaneh Agha-Hosseini - (Author)
  • Heike Görgens - (Author)
  • Maria Jatzwauk - (Author)
  • Stephanie von Kannen - (Author)
  • Barbara Noack - , Department of Prosthodontics (Author)
  • Uwe Eckelt - (Author)
  • Per Hoffmann - (Author)
  • Samira B Shabestari - (Author)
  • Parvin Mehdipour - (Author)

Details

Original languageEnglish
Pages (from-to)885-7
Number of pages3
JournalInternational journal of dermatology : official organ of the International Society of Dermatology
Volume53
Issue number7
Publication statusPublished - Jul 2014
Peer-reviewedYes

External IDs

PubMed 23556547
Scopus 84902828013
ORCID /0000-0002-0423-7107/work/147142740

Keywords

Sustainable Development Goals

Keywords

  • Adult, Base Sequence, Cathepsin C/genetics, Chromosomes, Human, Pair 11/genetics, DNA Mutational Analysis, Female, Homozygote, Humans, Iran, Male, Papillon-Lefevre Disease/genetics, Pedigree, Sequence Deletion, Young Adult