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Mutations in renal ion transporters cause Gitelman's and Bartter's syndromes of inherited hypokalemic alkalosis.

Advances in nephrology from the Necker Hospital - 1 Jan 1997

Simon D B, Lifton R P

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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PMID: 9408455

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Mutations in renal ion transporters cause Gitelman's and Bartter's syndromes of inherited hypokalemic alkalosis.PMID 9408455Read ↗

Mutations in Na(K)Cl transporters in Gitelman's and Bartter's syndromes.Semantic proximity Read ↗

Ion transporter mutations in Gitelman's and Bartter's syndromes.Semantic proximity Read ↗

Genetic disorders of renal electrolyte transport.Semantic proximity Read ↗

Gitelman's variant of Barter's syndrome, inherited hypokalaemic alkalosis, is caused by mutations in the thiazide-sensitive Na–Cl cotransporterSemantic proximity Read ↗

The molecular basis of inherited hypokalemic alkalosis: Bartter's and Gitelman's syndromes.Semantic proximity Read ↗

Inherited forms of renal hypomagnesemia: an updateSemantic proximity Read ↗

[Electrolyte disorders as a hallmark of monogenetic diseases].Semantic proximity Read ↗

Bartter's syndrome, hypokalaemic alkalosis with hypercalciuria, is caused by mutations in the Na-K-2Cl cotransporter NKCC2.Semantic proximity Read ↗

Bartter's and Gitelman's syndromes: from gene to clinic.Semantic proximity Read ↗

Clinical Features and Unusual Heterozygous Mutations in Patients with Renal Hypokalemia.Semantic proximity Read ↗

Potassium-related inherited tubulopathies.Semantic proximity Read ↗

Molecular pathophysiology of Bartter's and Gitelman's syndromes.Semantic proximity Read ↗

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