Inherited salt‐losing tubulopathy: An old condition but a new category of tubulopathy
Author:
Affiliation:
1. Department of PediatricsKobe University Graduate School of Medicine KobeJapan
2. Kitasato University School of Medicine SagamiharaJapan
3. Department of Nephrology Tokyo Metropolitan Children’s Medical Center Fuchu Japan
Publisher
Wiley
Subject
Pediatrics, Perinatology, and Child Health
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1111/ped.14089
Reference58 articles.
1. Mutations in the chloride channel gene, CLCNKB, cause Bartter's syndrome type III
2. Bartter's syndrome, hypokalaemic alkalosis with hypercalciuria, is caused by mutations in the Na–K–2CI cotransporter NKCC2
3. Genetic heterogeneity of Barter's syndrome revealed by mutations in the K+ channel, ROMK
4. Gitelman's variant of Barter's syndrome, inherited hypokalaemic alkalosis, is caused by mutations in the thiazide-sensitive Na–Cl cotransporter
5. Mutation of BSND causes Bartter syndrome with sensorineural deafness and kidney failure
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