APA (7th ed.) Citation

Singin, B., Donbaloğlu, Z., Çetiner, E. B., Çetin, K., Zarif, N. Ö., Çelik, K., . . . Parlak, M. (2026). A Rare Cause of Neonatal Salt Wasting Syndrome: Clinical Management of a Case Diagnosed with Pseudohypoaldosteronism due to a Novel Homozygous Variant in the SCNN1B Gene. Journal of Clinical Research in Pediatric Endocrinology, 18, 54. https://doi.org/10.4274/jcrpe.galenos.2024.2024-10-5

Chicago Style (17th ed.) Citation

Singin, Berna, et al. "A Rare Cause of Neonatal Salt Wasting Syndrome: Clinical Management of a Case Diagnosed with Pseudohypoaldosteronism Due to a Novel Homozygous Variant in the SCNN1B Gene." Journal of Clinical Research in Pediatric Endocrinology 18 (2026): 54. https://doi.org/10.4274/jcrpe.galenos.2024.2024-10-5.

MLA (9th ed.) Citation

Singin, Berna, et al. "A Rare Cause of Neonatal Salt Wasting Syndrome: Clinical Management of a Case Diagnosed with Pseudohypoaldosteronism Due to a Novel Homozygous Variant in the SCNN1B Gene." Journal of Clinical Research in Pediatric Endocrinology, vol. 18, 2026, p. 54, https://doi.org/10.4274/jcrpe.galenos.2024.2024-10-5.