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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 14, 2025. (Total: 235269Documents)
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Records 1 - 4 (of 4 Records)

Query Trace: Liddle Syndrome and SCNN1G[original query]
A Novel Frameshift Mutation of SCNN1G Causing Liddle Syndrome with Normokalemia.
American journal of hypertension 2019 4 32 (8): 752-758.
Fan Peng, Zhao Yu-Mo, Zhang Di, Liao Ying, Yang Kun-Qi, Tian Tao, Lou Ying, Luo Fang, Ma Wen-Jun, Zhang Hui-Min, Song Lei, Cai Jun, Liu Ya-Xin, Zhou Xian-Lia
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 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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