İŞLEYEN, F.; ULUBAŞ IŞIK, D.; KAVURT, A. S.; BAYRAM, A.; BAŞ, A. Y.; 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. Medical Science and Discovery, [S. l.], v. 10, n. 10, p. 935–938, 2023. DOI: 10.36472/msd.v10i10.1060. Disponível em: https://medscidiscovery.com/index.php/msd/article/view/1060. Acesso em: 29 feb. 2024.