HuGE Literature Finder
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| Genotype and clinical characteristics of congenital long QT syndrome in Thailand. Indian pacing and electrophysiology journal 2018 7 18 (5): 165-171. Saprungruang Ankavipar, Khongphatthanayothin Apichai, Mauleekoonphairoj John, Wandee Pharawee, Kanjanauthai Supaluck, Bhuiyan Zahurul A, Wilde Arthur A M, Poovorawan Yo |
| An East Asian Common Variant Vinculin P.Asp841His Was Associated With Sudden Unexplained Nocturnal Death Syndrome in the Chinese Han Population. Journal of the American Heart Association 2017 Apr 6 (4): . Cheng Jianding, Kyle John W, Lang Di, Wiedmeyer Brandi, Guo Jian, Yin Kun, Huang Lei, Vaidyanathan Ravi, Su Terry, Makielski Jonathan |
| Mutational analysis of SCN5A gene in long QT syndrome. Meta gene 2015 Dec 6 26-35. Qureshi Sameera Fatima, Ali Altaf, John Princy, Jadhav Amol P, Venkateshwari Ananthapur, Rao Hygriv, Jayakrishnan M P, Narasimhan Calambur, Shenthar Jayaprakash, Thangaraj Kumarasamy, Nallari Pratib |
| Cardiac channel molecular autopsy: insights from 173 consecutive cases of autopsy-negative sudden unexplained death referred for postmortem genetic testing. Mayo Clinic proceedings 2012 Jun 87 (6): 524-39. Tester David J, Medeiros-Domingo Argelia, Will Melissa L, Haglund Carla M, Ackerman Michael |
| Prospective, population-based long QT molecular autopsy study of postmortem negative sudden death in 1 to 40 year olds. Heart rhythm : the official journal of the Heart Rhythm Society 2011 Mar 8 (3): 412-9. Skinner Jonathan R, Crawford Jackie, Smith Warren, Aitken Andrew, Heaven David, Evans Cary-Anne, Hayes Ian, Neas Katherine R, Stables Simon, Koelmeyer Timothy, Denmark Lloyd, Vuletic Jane, Maxwell Fraser, White Kate, Yang Tao, Roden Dan M, Leren Trond P, Shelling Andrew, Love Donald R, |
| A common cardiac sodium channel variant associated with sudden infant death in African Americans, SCN5A S1103Y. The Journal of clinical investigation 2006 Feb 116 (2): 430-5. Plant Leigh D, Bowers Peter N, Liu Qianyong, Morgan Thomas, Zhang Tingting, State Matthew W, Chen Weidong, Kittles Rick A, Goldstein Steve A |
| Double SCN5A mutation underlying asymptomatic Brugada syndrome. Heart rhythm : the official journal of the Heart Rhythm Society 2005 Mar 2 (3): 285-92. Yokoi Hisataka, Makita Naomasa, Sasaki Koji, Takagi Yasuhiro, Okumura Yasuo, Nishino Tetsuo, Makiyama Takeru, Kitabatake Akira, Horie Minoru, Watanabe Ichiro, Tsutsui Hiroyu |
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