Mutations in a novel gene, encoding a single transmembrane domain protein are associated with familial glucocorticoid deficiency type 2

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

Contributors

  • Louise A. Metherell - , Barts Health NHS Trust (Author)
  • Sadani Cooray - , Barts Health NHS Trust (Author)
  • Angela Huebner - , Department of Paediatrics (Author)
  • Franz Ruschendorf - , Max Delbrück Center for Molecular Medicine (MDC) (Author)
  • Danielle Naville - , Hôpital Debrousse (Author)
  • Martine Begeot - , Hôpital Debrousse (Author)
  • Adrian J.L. Clark - , QMUL (Author)

Details

Original languageEnglish
Pages (from-to)889-890
Number of pages2
JournalEndocrine research
Volume30
Issue number4
Publication statusPublished - 2004
Peer-reviewedYes

External IDs

Scopus 11244299548
PubMed 15666841

Keywords