İşleyen, F., D. Ulubaş Işık, A. S. Kavurt, A. Bayram, A. Y. Baş, and N. Demirel. “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”. 2023. Medical Science and Discovery, vol. 10, no. 10, Nov. 2023, pp. 935-8, doi:10.36472/msd.v10i10.1060.