Human Genome Epidemiology Literature Finder
Records 1 - 3 (of 3 Records) |
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 |
A frameshift mutation in the SCNN1B gene in a family with Liddle syndrome: A case report and systematic review. Molecular medicine reports 2023 12 29 (2): . Yiting Lu, Xinchang Liu, Lin Sun, Di Zhang, Peng Fan, Kunqi Yang, Lin Zhang, Yaxin Liu, Xianliang Zh |
Reverse Phenotypes of Patients with Genetically Confirmed Liddle's Syndrome. Clinical journal of the American Society of Nephrology : CJASN 2024 1 . Granhøj Jeff, Nøhr Thomas K, Hinrichs Gitte R, Rasmussen Maria, Svenningsen P |
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