Genetic basis of Bartter syndrome in Korea-Reference-Cited by-同舟云学术

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Genetic basis of Bartter syndrome in Korea

Published:2011-08-23 Issue:4 Volume:27 Page:1516-1521
ISSN:0931-0509
Container-title:Nephrology Dialysis Transplantation
language:en
Short-container-title:Nephrology Dialysis Transplantation

Author:

Lee B. H.,Cho H. Y.,Lee H.,Han K. H.,Kang H. G.,Ha I. S.,Lee J. H.,Park Y. S.,Shin J. I.,Lee D.-Y.,Kim S.-Y.,Choi Y.,Cheong H. I.

Publisher

Oxford University Press (OUP)

Subject

Transplantation,Nephrology

Link

http://academic.oup.com/ndt/article-pdf/27/4/1516/7634349/gfr475.pdf

Reference35 articles.

1. Hyperplasia of the juxtaglomerular complex with hyperaldosteronism and hypokalemic alkalosis

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. Mutations in the chloride channel gene, CLCNKB, cause Bartter's syndrome type III

5. Mutation of BSND causes Bartter syndrome with sensorineural deafness and kidney failure

Cited by 45 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Untangling the Uncertain Role of Overactivation of the Renin–Angiotensin–Aldosterone System with the Aging Process Based on Sodium Wasting Human Models;International Journal of Molecular Sciences;2024-08-28

2. Bartter Syndrome Presenting as Arginine-Vasopressin Resistance: A Report of 2 Cases;AM J CASE REP;2024

3. Coexistence of Neonatal Bartter Syndrome and Congenital Cutis Laxa, in which a new mutation in SLC12A1 was identified;Medical Science and Discovery;2023-10-30

4. A novel homozygous CLCNKB variant: An early presentation of classic Bartter syndrome in a neonate;Birth Defects Research;2023-08-16

5. Long-term outcome of Bartter syndrome in 54 patients: A multicenter study in Korea;Frontiers in Medicine;2023-03-13

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