Liu, L., Hayashi, K., Kaneda, T., Ino, H., Fujino, N., Uchiyama, K., … Yamagishi, M. (2013). A novel mutation in the transmembrane nonpore region of the KCNH2 gene causes severe clinical manifestations of long QT syndrome. Heart Rhythm, 10(1), 61–67. https://doi.org/10.1016/j.hrthm.2012.09.053

Liu, Li, Kenshi Hayashi, Tomoya Kaneda, Hidekazu Ino, Noboru Fujino, Katsuharu Uchiyama, Tetsuo Konno, et al. “A novel mutation in the transmembrane nonpore region of the KCNH2 gene causes severe clinical manifestations of long QT syndrome.” Heart Rhythm 10, no. 1 (January 2013): 61–67. https://doi.org/10.1016/j.hrthm.2012.09.053.

Liu L, Hayashi K, Kaneda T, Ino H, Fujino N, Uchiyama K, et al. A novel mutation in the transmembrane nonpore region of the KCNH2 gene causes severe clinical manifestations of long QT syndrome. Heart Rhythm. 2013 Jan;10(1):61–7.

Liu, Li, et al. “A novel mutation in the transmembrane nonpore region of the KCNH2 gene causes severe clinical manifestations of long QT syndrome.” Heart Rhythm, vol. 10, no. 1, Elsevier BV, Jan. 2013, pp. 61–67. Crossref, doi:10.1016/j.hrthm.2012.09.053.

Liu L, Hayashi K, Kaneda T, Ino H, Fujino N, Uchiyama K, Konno T, Tsuda T, Kawashiri M-A, Ueda K, Higashikata T, Shuai W, Kupershmidt S, Higashida H, Yamagishi M. A novel mutation in the transmembrane nonpore region of the KCNH2 gene causes severe clinical manifestations of long QT syndrome. Heart Rhythm. Elsevier BV; 2013 Jan;10(1):61–67.