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

Pub. Date : 1998 Jan

PMID : 9502574






1 Functional Relationships(s)
Download
Sentence
Compound Name
Protein Name
Organism
1 Two genes, the gene encoding the furosemide-sensitive apical Na-K-2Cl cotransporter (NKCC2) and the gene encoding the luminal inwardly-rectifying potassium channel Kir 1.1 (ROMK), have been reported to cause the neonatal subtype of Bartter syndrome. Furosemide solute carrier family 12 member 1 Homo sapiens