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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. BMC Med Genet. 2014 Mar 7;15:31. doi: 10.1186/1471-2350-15-31. BMC Med Genet. 2014. PMID: 24606995 Free PMC article.
Mutations in calmodulin cause ventricular tachycardia and sudden cardiac death.
Nyegaard M, Overgaard MT, Søndergaard MT, Vranas M, Behr ER, Hildebrandt LL, Lund J, Hedley PL, Camm AJ, Wettrell G, Fosdal I, Christiansen M, Børglum AD. Nyegaard M, et al. Among authors: christiansen m. Am J Hum Genet. 2012 Oct 5;91(4):703-12. doi: 10.1016/j.ajhg.2012.08.015. Am J Hum Genet. 2012. PMID: 23040497 Free PMC article.
Family history of premature death and risk of early onset cardiovascular disease.
Ranthe MF, Carstensen L, Oyen N, Tfelt-Hansen J, Christiansen M, McKenna WJ, Wohlfahrt J, Melbye M, Boyd HA. Ranthe MF, et al. Among authors: christiansen m. J Am Coll Cardiol. 2012 Aug 28;60(9):814-21. doi: 10.1016/j.jacc.2012.06.018. J Am Coll Cardiol. 2012. PMID: 22917005 Free article.
956 results