Genetics of ACTH insensitivity syndromes

Research output: Contribution to journalResearch articleContributedpeer-review

Contributors

  • J. L.A. Clark - , Queen Mary University of London (Author)
  • L. A. Metherell - , Queen Mary University of London (Author)
  • D. Naville - , INSERM - Institut national de la santé et de la recherche médicale (Author)
  • M. Begeot - , INSERM - Institut national de la santé et de la recherche médicale (Author)
  • A. Huebner - , Department of Paediatrics (Author)

Abstract

The last decade has seen remarkable progress in our understanding of the genetic causes of these potentially lethal conditions. Clearly, other genes that cause FGD remain to be discovered, and further work is required on the functions of MRAP and ALADIN in the expectation that they will provide insights into essential biological processes and perhaps identify key therapeutic strategies and targets for these diseases.

Details

Original languageEnglish
Pages (from-to)247-249
Number of pages3
JournalAnnales d'endocrinologie
Volume66
Issue number3
Publication statusPublished - Jun 2005
Peer-reviewedYes

External IDs

Scopus 18944397267
PubMed 15988386

Keywords