1. Liatakis, Ioannis, Pantou, Malena P, Gourzi, Polyxeni, Efremidis, Michael, Letsas, Konstantinos P. 2021. KCNE2 gene mutation and Brugada syndrome. In Journal of electrocardiology, 65, 143-145. doi:10.1016/j.jelectrocard.2021.01.022. https://pubmed.ncbi.nlm.nih.gov/33626434/
2. Kapplinger, Jamie D, Tester, David J, Salisbury, Benjamin A, Wilde, Arthur A M, Ackerman, Michael J. 2009. Spectrum and prevalence of mutations from the first 2,500 consecutive unrelated patients referred for the FAMILION long QT syndrome genetic test. In Heart rhythm, 6, 1297-303. doi:10.1016/j.hrthm.2009.05.021. https://pubmed.ncbi.nlm.nih.gov/19716085/
3. Splawski, I, Shen, J, Timothy, K W, Vincent, G M, Keating, M T. . Spectrum of mutations in long-QT syndrome genes. KVLQT1, HERG, SCN5A, KCNE1, and KCNE2. In Circulation, 102, 1178-85. doi:. https://pubmed.ncbi.nlm.nih.gov/10973849/
4. Lisewski, Ulrike, Köhncke, Clemens, Schleussner, Leonhard, Abbott, Geoffrey W, Roepke, Torsten K. 2020. Hypochlorhydria reduces mortality in heart failure caused by Kcne2 gene deletion. In FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 34, 10699-10719. doi:10.1096/fj.202000013RR. https://pubmed.ncbi.nlm.nih.gov/32584506/
5. Kundu, Pallob, Ciobotaru, Andrea, Foroughi, Sina, Stefani, Enrico, Eghbali, Mansoureh. 2008. Hormonal regulation of cardiac KCNE2 gene expression. In Molecular and cellular endocrinology, 292, 50-62. doi:10.1016/j.mce.2008.06.003. https://pubmed.ncbi.nlm.nih.gov/18611433/
6. Yanglin, Pan, Lina, Zhao, Zhiguo, Liu, Jianhong, Wang, Daiming, Fan. 2006. KCNE2, a down-regulated gene identified by in silico analysis, suppressed proliferation of gastric cancer cells. In Cancer letters, 246, 129-38. doi:. https://pubmed.ncbi.nlm.nih.gov/16677757/
7. Song, Ming, Zhuge, Yixin, Tu, Yuqi, Liu, Jie, Liu, Wenjuan. 2024. The Multifunctional Role of KCNE2: From Cardiac Arrhythmia to Multisystem Disorders. In Cells, 13, . doi:10.3390/cells13171409. https://pubmed.ncbi.nlm.nih.gov/39272981/
智鼠故事 
