Human Genome Epidemiology Literature Finder
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Records 1 - 9 (of 9 Records) |
| Query Trace: Syndrome and SCNN1G[original query] |
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| Association of sodium channel gamma-subunit promoter variant with blood pressure. Hypertension 2001 Jul 38 (1): 86-9. Iwai N, Baba S, Mannami T, Katsuya T, Higaki J, Ogihara T, Ogata J |
| Six missense mutations of the epithelial sodium channel beta and gamma subunits in Japanese hypertensives. Hypertension research : official journal of the Japanese Society of Hypertension 2004 May 27 (5): 333-8. Kamide Kei, Tanaka Chihiro, Takiuchi Shin, Miwa Yoshikazu, Yoshii Masayoshi, Horio Takeshi, Kawano Yuhei, Miyata Toshiyu |
| Common variants in genes underlying monogenic hypertension and hypotension and blood pressure in the general population. Hypertension 2008 Jun 51 (6): 1658-64. Tobin Martin D, Tomaszewski Maciej, Braund Peter S, Hajat Cother, Raleigh Stuart M, Palmer Thomas M, Caulfield Mark, Burton Paul R, Samani Nilesh |
| Genetic analysis of Rwandan patients with cystic fibrosis-like symptoms: identification of novel cystic fibrosis transmembrane conductance regulator and epithelial sodium channel gene variants. Chest 2009 May 135 (5): 1233-42. Mutesa Léon, Azad Abul Kalam, Verhaeghe Catherine, Segers Karin, Vanbellinghen Jean-François, Ngendahayo Louis, Rusingiza Emmanuel Kamanzi, Mutwa Philippe Rutwaza, Rulisa Stephen, Koulischer Lucien, Cassiman Jean-Jacques, Cuppens Harry, Bours Vince |
| Analysis of the genes involved in Mendelian forms of low-renin hypertension in Chinese early-onset hypertensive patients. Journal of hypertension 2017 Sep . Liu Kai, Qin Fang, Sun Xiaolu, Zhang Yang, Wang Jizheng, Wu Yajie, Ma Wenjun, Wang Wei, Wu Xueyi, Qin Ying, Zhang Huimin, Zhou Xianliang, Wu Haiying, Hui Rutai, Zou Yubao, Jiang Xiongjing, Song L |
| 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 |
- Page last reviewed:Feb 1, 2024
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