Title : Classification and rescue of ROMK mutations underlying hyperprostaglandin E syndrome/antenatal Bartter syndrome.

Pub. Date : 2003 Sep

PMID : 12911542






2 Functional Relationships(s)
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1 BACKGROUND: Mutations in the renal K+ channel ROMK (Kir 1.1) cause hyperprostaglandin E syndrome/antenatal Bartter syndrome (HPS/aBS), a severe tubular disorder leading to renal salt and water wasting. Water potassium inwardly rectifying channel subfamily J member 1 Homo sapiens
2 BACKGROUND: Mutations in the renal K+ channel ROMK (Kir 1.1) cause hyperprostaglandin E syndrome/antenatal Bartter syndrome (HPS/aBS), a severe tubular disorder leading to renal salt and water wasting. Water potassium inwardly rectifying channel subfamily J member 1 Homo sapiens