AHMAD, N.; ATIYAH, M.; AL GHAMDI, B. A.; AL ENIZI, H. F.; AL ZAHRANI, A. S. Pseudo hypoaldosteronism type 1B due to novel deletion mutation in SCNN1A gene. International Journal of Contemporary Pediatrics, [S. l.], v. 6, n. 6, p. 2705–2708, 2019. DOI: 10.18203/2349-3291.ijcp20194760. Disponível em: https://www.ijpediatrics.com/index.php/ijcp/article/view/2846. Acesso em: 23 oct. 2025.