Coexistence of Neonatal Bartter Syndrome and Congenital Cutis Laxa, in which a new mutation in SLC12A1 was identified

İŞLEYEN F., ULUBAŞ IŞIK D., KAVURT A. S., BAYRAM A., BAŞ A. Y., DEMİREL N.

Medical Science and Discovery, cilt.10, 2023 (Hakemli Dergi)