İşleyen F, Ulubaş Işık D, Kavurt AS, Bayram A, Baş AY, Demirel N. Coexistence of Neonatal Bartter Syndrome and Congenital Cutis Laxa, in which a new mutation in SLC12A1 was identified: Coexistence of Congenital Cutis Laxa and Neonatal Bartter Syndrome. Med Sci Discov [Internet]. 2023 Nov. 8 [cited 2024 Feb. 29];10(10):935-8. Available from: https://medscidiscovery.com/index.php/msd/article/view/1060