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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 25, 2025. (Total: 235671Documents)
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Records 1 - 3 (of 3 Records)

Query Trace: Hypokalemia and SCNN1B[original query]
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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