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Mutations in the Kv1.5 channel gene KCNA5 in cardiac arrest patients.
Nielsen NH, Winkel BG, Kanters JK, Schmitt N, Hofman-Bang J, Jensen HS, Bentzen BH, Sigurd B, Larsen LA, Andersen PS, Haunsø S, Kjeldsen K, Grunnet M, Christiansen M, Olesen SP. Nielsen NH, et al. Among authors: kanters jk. Biochem Biophys Res Commun. 2007 Mar 16;354(3):776-82. doi: 10.1016/j.bbrc.2007.01.048. Epub 2007 Jan 18. Biochem Biophys Res Commun. 2007. PMID: 17266934
[Short QT syndrome as an inherited condition].
Møller DV, Hedley PL, Olesen M, Kanters J, Svendsen JH, Christiansen M. Møller DV, et al. Ugeskr Laeger. 2011 Feb 7;173(6):420-4. Ugeskr Laeger. 2011. PMID: 21299935 Review. Danish.
Rare genetic variants previously associated with congenital forms of long QT syndrome have little or no effect on the QT interval.
Ghouse J, Have CT, Weeke P, Bille Nielsen J, Ahlberg G, Balslev-Harder M, Appel EV, Skaaby T, Olesen SP, Grarup N, Linneberg A, Pedersen O, Haunsø S, Hastrup Svendsen J, Hansen T, Kanters JK, Salling Olesen M. Ghouse J, et al. Among authors: kanters jk. Eur Heart J. 2015 Oct 1;36(37):2523-9. doi: 10.1093/eurheartj/ehv297. Epub 2015 Jul 9. Eur Heart J. 2015. PMID: 26159999
KCNE1 G38S polymorphism is not the cause of long QT syndrome.
Kanters JK, Olesen MS, Christiansen M. Kanters JK, et al. J Electrocardiol. 2016 Mar-Apr;49(2):249-50. doi: 10.1016/j.jelectrocard.2015.12.005. Epub 2015 Dec 12. J Electrocardiol. 2016. PMID: 26781364 No abstract available.
Numerous Brugada syndrome-associated genetic variants have no effect on J-point elevation, syncope susceptibility, malignant cardiac arrhythmia, and all-cause mortality.
Ghouse J, Have CT, Skov MW, Andreasen L, Ahlberg G, Nielsen JB, Skaaby T, Olesen SP, Grarup N, Linneberg A, Pedersen O, Vestergaard H, Haunsø S, Svendsen JH, Hansen T, Kanters JK, Olesen MS. Ghouse J, et al. Among authors: kanters jk. Genet Med. 2017 May;19(5):521-528. doi: 10.1038/gim.2016.151. Epub 2016 Oct 6. Genet Med. 2017. PMID: 27711072 Free article.
196 results