HuGE Literature Finder
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| Genome sequencing in a genetically elusive multigenerational long QT syndrome pedigree identifies a novel LQT2-causative deeply intronic KCNH2 variant. Heart rhythm 2022 2 19 (6): 998-1007. Tobert Kathryn E, Tester David J, Zhou Wei, Haglund-Turnquist Carla M, Giudicessi John R, Ackerman Michael |
| Genetic Variants on SCN5A, KCNQ1, and KCNH2 in Patients with Ventricular Arrhythmias during Acute Myocardial Infarction in a Chinese Population. Cardiology 2019 Nov 1-8. Wang Feng, Liu Yang, Liao Hongtao, Xue Yumei, Zhan Xianzhang, Fang Xianhong, Liang Yuanhong, Wei Wei, Rao Fang, Zhang Qianhuan, Deng Hai, Lin Yubi, Liu Fangzhou, Lin Weidong, Zhang Bin, Wu Shul |
| Mutation Analysis of KCNQ1, KCNH2 and SCN5A Genes in Taiwanese Long QT Syndrome Patients. International heart journal 2015 56 (4): 450-3. Chang Ya-Sian, Yang Yi-Wen, Lin Yen-Nien, Lin Kuo-Hung, Chang Kuan-Cheng, Chang Jan-Gow |
| Mutation analysis ion channel genes ventricular fibrillation survivors with coronary artery disease. Pacing and clinical electrophysiology : PACE 2011 Jun 34 (6): 742-9. Novotny Tomas, Kadlecova Jitka, Raudenska Martina, Bittnerova Alexandra, Andrsova Irena, Florianova Alena, Vasku Anna, Neugebauer Petr, Kozak Milan, Sepsi Milan, Krivan Lubomir, Gaillyova Renata, Spinar Jindri |
| Denaturing high-performance liquid chromatography screening of the long QT syndrome-related cardiac sodium and potassium channel genes and identification of novel mutations and single nucleotide polymorphisms. Journal of human genetics 2005 50 (9): 490-6. Lai Ling-Ping, Su Yi-Ning, Hsieh Fon-Jou, Chiang Fu-Tien, Juang Jyh-Ming, Liu Yen-Bin, Ho Yi-Lwun, Chen Wen-Jone, Yeh San-Jou, Wang Chun-Chieh, Ko Yu-Lin, Wu Tsu-Juey, Ueng Kwo-Chang, Lei Meng-Huan, Tsao Hsuan-Ming, Chen Shih-Ann, Lin Tin-Kwang, Wu Mei-Hwan, Lo Huey-Ming, Huang Shoei K Stephen, Lin Jiunn-L |
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