[1]
İşleyen, F., Ulubaş Işık, D., Kavurt, A.S., Bayram, A., Baş, A.Y. and Demirel, N. 2023. 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. Medical Science and Discovery. 10, 10 (Nov. 2023), 935–938. DOI:https://doi.org/10.36472/msd.v10i10.1060.