Mutation spectrum of Chinese patients with Bartter syndrome-Reference-Cited by-同舟云学术

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Mutation spectrum of Chinese patients with Bartter syndrome

Published:2017-09-27 Issue:60 Volume:8 Page:101614-101622
ISSN:1949-2553
Container-title:Oncotarget
language:en
Short-container-title:Oncotarget

Author:

Han Yue¹²,Lin Yi³,Sun Qing⁴,Wang Shujuan²,Gao Yanxia⁵,Shao Leping¹²

Affiliation:

1. Central Laboratory, Affiliated Hospital, Qingdao University, Qingdao 266003, P.R. China

2. Department of Nephrology, Affiliated Hospital, Qingdao University, Qingdao 266003, P.R. China

3. Pediatrics, Affiliated Hospital, Qingdao University, Qingdao 266003, P.R. China

4. Department of Nephrology, Qingdao Women and Children's Hospital, Qingdao University, Qingdao 266011, P.R. China

5. Department of Nephrology, Qingdao Branch of Qilu Hospital of Shandong University, Qingdao, Shandong 266000, P.R. China

Publisher

Impact Journals, LLC

Subject

Oncology

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1. Clinical, genetic characteristics and outcome of four Chinese patients with Bartter syndrome type 3: Further insight into a genotype-phenotype correlation;Molecular Genetics and Metabolism Reports;2024-09

2. Bartter syndrome in children: a series of eight cases from the Czech Republic and Slovakia;Česko-slovenská pediatrie;2024-04-01

3. Adult classic Bartter syndrome: a case report with 5-year follow-up and literature review;Endocrine Journal;2024

4. Long-read sequencing identifies a common transposition haplotype predisposing for CLCNKB deletions;Genome Medicine;2023-08-23

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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