Three novel missense mutations of WNK4, a kinase mutated in inherited hypertension, in Japanese hypertensives Implication of clinical phenotypes
Author:
Publisher
Oxford University Press (OUP)
Subject
Internal Medicine
Link
http://academic.oup.com/ajh/article-pdf/17/5/446/210057/17_5_446.pdf
Cited by 29 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. Novel variant WNK4 gene identified in early-onset severe hypertension: a case report;QJM: An International Journal of Medicine;2024-07-23
2. Novel Association of WNK4 Gene, Ala589Ser Polymorphism in Essential Hypertension, and Type 2 Diabetes Mellitus in Malaysia;Journal of Diabetes Research;2016
3. Comprehensive Assessment of the Association of WNK4 Polymorphisms with Hypertension: Evidence from a Meta-Analysis;Scientific Reports;2014-09-30
4. SPAK Deficiency Corrects Pseudohypoaldosteronism II Caused by WNK4 Mutation;PLoS ONE;2013-09-11
5. Physiology and Pathophysiology of the NaCl Co-Transporters in the Kidney;Seldin and Giebisch's The Kidney;2013
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