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.


Creative Commons License

Singin B., Donbaloğlu Z., Barsal Çetiner E., Çetin K., Özkan Zarif N., Çelik K., ...Daha Fazla

Journal of clinical research in pediatric endocrinology, 2024 (SCI-Expanded) identifier