Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Kirsten Salzgeber"'
Autor:
Walter Bonfig, Egbert Voss, Kirsten Salzgeber, C. Denzer, Gerhard Binder, Markus Bettendorf, Karl Otfried Schwab, Heinrich Schmidt, J. Wölfle, Desiree Dunstheimer, Martin Wabitsch, Helmuth-Günther Dörr, Nadja Schulze
Publikováno v:
Molecular and Cellular Pediatrics
Background Nonclassical congenital adrenal hyperplasia due to 21-hydroxylase deficiency is caused by mutations in the active 21-hydroxylase gene (CYP21A2). The clinical symptoms can vary greatly. To date, no systematic studies have been undertaken in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::69958778bb117de1b09fb34d589b8329
https://doi.org/10.1186/s40348-020-00100-w
https://doi.org/10.1186/s40348-020-00100-w
Autor:
Schreiner, Felix1 felix.schreiner@ukb.uni-bonn.de, Brack, Christoph2, Salzgeber, Kirsten3, Vorhoff, Walburga, Woelfle, Joachim1, Gohlke, Bettina1
Publikováno v:
European Journal of Pediatrics. Apr2008, Vol. 167 Issue 4, p479-481. 3p. 1 Chart.