Fingerprint
Dive into the research topics of 'CYP11B1 mutations causing congenital adrenal hyperplasia due to 11β- hydroxylase deficiency'. Together they form a unique fingerprint.- Sort by
- Weight
- Alphabetically
CYP11B1 mutations causing congenital adrenal hyperplasia due to 11β- hydroxylase deficiency
Stephan Geley, Klaus Kapelari, Karin Jöhrer, Michael Peter, Josef Glatzl, Heinrich Vierhapper, Siegfried Schwarz, Arno Helmberg, Wolfgang G. Sippell, Perrin C. White, Reinhard Kofler
Research output: Contribution to journal › Article › peer-review
114
Scopus
citations