Novel variant WNK4 gene identified in early-onset severe hypertension: a case report
Author:
Affiliation:
1. Department of Endocrinology and Metabolism, Institute of Endocrinology, NHC Key Laboratory of Diagnosis and Treatment of Thyroid Diseases, The First Hospital of China Medical University , Shenyang, P.R. China
Publisher
Oxford University Press (OUP)
Link
https://academic.oup.com/qjmed/advance-article-pdf/doi/10.1093/qjmed/hcae143/58653548/hcae143.pdf
Reference6 articles.
1. Genomics and precision medicine for clinicians and scientists in hypertension;Dominiczak;Hypertension,2017
2. Human hypertension caused by mutations in WNK kinases;Wilson;Science,2001
3. Three novel missense mutations of WNK4, a kinase mutated in inherited hypertension, in Japanese hypertensives: implication of clinical phenotypes;Kamide;Am J Hypertens,2004
4. Genetic screening for monogenic hypertension in hypertensive individuals in a clinical setting;Bao;J Med Genet,2020
5. WNK4 kinase: from structure to physiology;Murillo-de-Ozores;Am J Physiol Renal Physiol,2021
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