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1998•Pediatric NephrologyRequires access

Two novel mutations of the gene for Kir 1.1 (ROMK) in neonatal Bartter syndrome

Martin Vollmer, Martin Koehrer, Rezan Topaloğlu, Brigitte Strahm, Heymut Omran, Friedhelm Hildebrandt

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Key concepts: Bartter syndrome, Bartter's syndrome, Endocrinology, Medicine, Internal medicine, Gene, Furosemide, Aldosterone

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Two novel mutations of the gene for Kir 1.1 (ROMK) in neonatal Bartter syndrome — Research Paper | ScholarLens