[1]
F. İşleyen, 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”, Med Sci Discov, vol. 10, no. 10, pp. 935–938, Nov. 2023.