Pseudohypoaldosteronism/geneticsRefine your research by the most used items
Author / Editor
- Dirlewanger, Mijam (1)
- Girardin, Eric (1)
- Huser, Delphine (1)
- Schild, Laurent (1)
- Schwitzgebel Luscher, Valérie (1)
- Zennaro, Maria-Christina (1)
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remove all| Title | Authors / Editors | Date | |
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A homozygous missense mutation in SCNN1A is responsible for a transient neonatal form of pseudohypoaldosteronism type 1 | Dirlewanger, Mijam; Huser, Delphine; Zennaro, Maria-Christina; Girardin, Eric; ... Schwitzgebel Luscher, Valérie | 2011 |
