Genetics of ACTH insensitivity syndromes
Research output: Contribution to journal › Research article › Contributed › peer-review
Contributors
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 language | English |
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Pages (from-to) | 247-249 |
Number of pages | 3 |
Journal | Annales d'endocrinologie |
Volume | 66 |
Issue number | 3 |
Publication status | Published - Jun 2005 |
Peer-reviewed | Yes |
External IDs
Scopus | 18944397267 |
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PubMed | 15988386 |