Patients With Biallelic Mutations in the Chloride Channel Gene CLCNKB: Long-Term Management and Outcome-Reference-Cited by-同舟云学术

Patients With Biallelic Mutations in the Chloride Channel Gene CLCNKB: Long-Term Management and Outcome

Published:2007-01 Issue:1 Volume:49 Page:91-98
ISSN:0272-6386
Container-title:American Journal of Kidney Diseases
language:en
Short-container-title:American Journal of Kidney Diseases

Author:

Bettinelli Alberto,Borsa Nicolò,Bellantuono Rosa,Syrèn Marie-Louise,Calabrese Raffaele,Edefonti Alberto,Komninos John,Santostefano Marisa,Beccaria Luciano,Pela Ivana,Bianchetti Mario G.,Tedeschi Silvana

Publisher

Elsevier BV

Subject

Nephrology

Reference24 articles.

1. Mutations in the chloride channel gene, CLCNKB, cause Bartter’s syndrome type III;Simon;Nat Genet,1997

2. Bartter syndrome;Heberth;Curr Opin Nephrol Hypertens,2003

3. Bartter’s and Gitelman’s syndromes: Their relationship to the actions of loop and thiazide diuretics;Unwin;Curr Opin Pharmacol,2006

4. Mutations in the chloride channel gene CLCNKB as a cause of classic Bartter syndrome;Konrad;J Am Soc Nephrol,2000

5. Clinical presentation of genetically defined patients with hypokalemic salt-losing tubulopathies;Peters;Am J Med,2002

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