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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Dec 12, 2024. (Total: 234319Documents)
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Records 1 - 4 (of 4 Records)

Query Trace: Liddle Syndrome and SCNN1B[original query]
Premature Stroke Secondary to Severe Hypertension Results from Liddle Syndrome Caused by a Novel SCNN1B Mutation.
Kidney & blood pressure research 2020 7 45 (4): 603-611.
Fan Peng, Zhang Di, Pan Xiao-Cheng, Yang Kun-Qi, Zhang Qiong-Yu, Lu Yi-Ting, Zhang Ying, Liu Xue-Ying, Ma Wen-Jun, Zhang Hui-Min, Song Lei, Cai Jun, Liu Ya-Xin, Zhou Xian-Lia
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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