Human Genome Epidemiology Literature Finder
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Query Trace: Hypokalemia and SCNN1B[original query] |
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A Novel Frame-Shift Mutation in SCNN1B Identified in a Chinese Family Characterized by Early-Onset Hypertension. Frontiers in cardiovascular medicine 2022 7 9 896564. Lu Yi-Ting, Liu Xin-Chang, Zhou Ze-Ming, Zhang Di, Sun Lin, Zhang Ying, Fan Peng, Zhang Lin, Liu Ya-Xin, Luo Fang, Zhou Xian-Lia |
- Page last reviewed:Feb 1, 2023
- Page last updated:May 22, 2023
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