Genotype-phenotype correlations in children and adolescents with nonclassical congenital adrenal hyperplasia due to 21-hydroxylase deficiency
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 Germany.
Guardado en:
| Autores principales: | , , , , , , , , , , , , |
|---|---|
| Formato: | Article (Journal) |
| Lenguaje: | inglés |
| Publicado: |
09 July 2020
|
| In: |
Molecular and Cellular Pediatrics
Year: 2020, Volumen: 7, Pages: 1-7 |
| ISSN: | 2194-7791 |
| DOI: | 10.1186/s40348-020-00100-w |
| Acceso en línea: | Verlag, kostenfrei, Volltext: https://doi.org/10.1186/s40348-020-00100-w Verlag, kostenfrei, Volltext: https://link.springer.com/article/10.1186/s40348-020-00100-w 
|
| Notas de Autor: | Helmuth-Günther Dörr, Nadja Schulze, Markus Bettendorf, Gerhard Binder, Walter Bonfig, Christian Denzer, Desiree Dunstheimer, Kirsten Salzgeber, Heinrich Schmidt, Karl Otfried Schwab, Egbert Voss, Martin Wabitsch and Joachim Wölfle |
Search Result 1