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Mutations in Danish patients with long QT syndrome and the identification of a large founder family with p.F29L in KCNH2.
Christiansen M, Hedley PL, Theilade J, Stoevring B, Leren TP, Eschen O, Sørensen KM, Tybjærg-Hansen A, Ousager LB, Pedersen LN, Frikke-Schmidt R, Aidt FH, Hansen MG, Hansen J, Bloch Thomsen PE, Toft E, Henriksen FL, Bundgaard H, Jensen HK, Kanters JK. Christiansen M, et al. Among authors: jensen hk. BMC Med Genet. 2014 Mar 7;15:31. doi: 10.1186/1471-2350-15-31. BMC Med Genet. 2014. PMID: 24606995 Free PMC article.
T(peak)T(end) interval in long QT syndrome.
Kanters JK, Haarmark C, Vedel-Larsen E, Andersen MP, Graff C, Struijk JJ, Thomsen PE, Christiansen M, Jensen HK, Toft E. Kanters JK, et al. Among authors: jensen hk. J Electrocardiol. 2008 Nov-Dec;41(6):603-8. doi: 10.1016/j.jelectrocard.2008.07.024. Epub 2008 Sep 25. J Electrocardiol. 2008. PMID: 18822425
The prevalence of mutations in KCNQ1, KCNH2, and SCN5A in an unselected national cohort of young sudden unexplained death cases.
Winkel BG, Larsen MK, Berge KE, Leren TP, Nissen PH, Olesen MS, Hollegaard MV, Jespersen T, Yuan L, Nielsen N, Haunsø S, Svendsen JH, Wang Y, Kristensen IB, Jensen HK, Tfelt-Hansen J, Banner J. Winkel BG, et al. Among authors: jensen hk. J Cardiovasc Electrophysiol. 2012 Oct;23(10):1092-8. doi: 10.1111/j.1540-8167.2012.02371.x. Epub 2012 Aug 6. J Cardiovasc Electrophysiol. 2012. PMID: 22882672
322 results