Singin, B. Et Al. 2024. 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 .

Singin, B., Donbaloğlu, Z., Barsal Çetiner, E., Çetin, K., Özkan Zarif, N., Çelik, K., ... Mıhçı, E.(2024). 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 .

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 , 2024

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 , 2024

Singin, B. Et Al. (2024) . "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 .

@article{article, author={Berna Singin Et Al. }, title={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={Journal of clinical research in pediatric endocrinology}, year=2024}