Human Genome Epidemiology Literature Finder
Records 1 - 7 (of 7 Records) |
Query Trace: Syndrome and KCND3[original query] |
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Mutations in the genes KCND2 and KCND3 encoding the ion channels Kv4.2 and Kv4.3, conducting the cardiac fast transient outward current (ITO,f), are not a frequent cause of long QT syndrome. Clinica chimica acta; international journal of clinical chemistry 2005 Jan 351 (1-2): 95-100. Frank-Hansen Rune, Larsen Lars Allan, Andersen Paal, Jespersgaard Cathrine, Christiansen Micha |
Transient outward current (I(to)) gain-of-function mutations in the KCND3-encoded Kv4.3 potassium channel and Brugada syndrome. Heart rhythm : the official journal of the Heart Rhythm Society 2011 Jul 8 (7): 1024-32. Giudicessi John R, Ye Dan, Tester David J, Crotti Lia, Mugione Alessandra, Nesterenko Vladislav V, Albertson Richard M, Antzelevitch Charles, Schwartz Peter J, Ackerman Michael |
Novel mutations in the KCND3-encoded Kv4.3 K+ channel associated with autopsy-negative sudden unexplained death. Human mutation 2012 Feb . Giudicessi JR, Ye D, Kritzberger CJ, Nesterenko VV, Tester DJ, Antzelevitch C, Ackerman MJ |
Sodium current and potassium transient outward current genes in Brugada syndrome: screening and bioinformatics. The Canadian journal of cardiology 0 28 (2): 196-200. Holst Anders G, Saber Siamak, Houshmand Massoud, Zaklyazminskaya Elena V, Wang Yinman, Jensen Henrik Kjærulf, Refsgaard Lena, Haunsø Stig, Svendsen Jesper Hastrup, Olesen Morten S, Tfelt-Hansen Jac |
Evaluation of genes encoding for the transient outward current (Ito) identifies the KCND2 gene as a cause of J-wave syndrome associated with sudden cardiac death. Circulation. Cardiovascular genetics 2014 Dec 7 (6): 782-9. Perrin Mark J, Adler Arnon, Green Sharon, Al-Zoughool Foad, Doroshenko Petro, Orr Nathan, Uppal Shaheen, Healey Jeff S, Birnie David, Sanatani Shubhayan, Gardner Martin, Champagne Jean, Simpson Chris, Ahmad Kamran, van den Berg Maarten P, Chauhan Vijay, Backx Peter H, van Tintelen J Peter, Krahn Andrew D, Gollob Michael |
Gene mutational analysis in a cohort of Chinese children with unexplained epilepsy: Identification of a new KCND3 phenotype and novel genes causing Dravet syndrome. Seizure 2019 2 66 26-30. Wang Jiaping, Wen Yongxin, Zhang Qingping, Yu Shujie, Chen Yan, Wu Xiru, Zhang YueHua, Bao Xinh |
Susceptibility to Ventricular Arrhythmias Resulting from Mutations in FKBP1B, PXDNL, and SCN9A Evaluated in hiPSC Cardiomyocytes. Stem cells international 2020 9 2020 8842398. Barajas-Martinez Hector, Smith Maya, Hu Dan, Goodrow Robert J, Puleo Colleen, Hasdemir Can, Antzelevitch Charles, Pfeiffer Ryan, Treat Jacqueline A, Cordeiro Jonathan |
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