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. - Singin, Berna; Donbaloğlu, Zeynep; Çetiner, Ebru Barsal; Çetin, Kürşat; Zarif, Nurten Özkan; Çelik, Kıymet; Mıhçı, Ercan; Clark, Özden Altıok; Tuhan, Hale; Parlak, Mesut (Journal of Clinical Research in Pediatric Endocrinology, 2026)