The triple A syndrome is due to mutations in ALADIN, a novel member of the nuclear pore complex

Research output: Contribution to journal › Research article › Contributed › peer-review

Contributors

  • A Huebner - , Department of Paediatrics (Author)
  • AM Kaindl - , TUD Dresden University of Technology, Charité – Universitätsmedizin Berlin (Author)
  • Klaus-Peter Knobeloch - , Free University of Berlin (Author)
  • H Petzold - , TUD Dresden University of Technology (Author)
  • P Mann - , TUD Dresden University of Technology (Author)
  • K Koehler - , Department of Paediatrics (Author)

Details

Original languageEnglish
Pages (from-to)891-899
Number of pages9
JournalEndocrine research
Volume30
Issue number4
Publication statusPublished - Nov 2004
Peer-reviewedYes

External IDs

ORCID /0000-0002-9407-1410/work/90094104
PubMed 15666842
Scopus 11244262589