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3. Spectrum and prevalence of mutations from the first 2,500 consecutive unrelated patients referred for the FAMILION long QT syndrome genetic test. Kapplinger JD; Tester DJ; Salisbury BA; Carr JL; Harris-Kerr C; Pollevick GD; Wilde AA; Ackerman MJ Heart Rhythm; 2009 Sep; 6(9):1297-303. PubMed ID: 19716085 [TBL] [Abstract][Full Text] [Related]
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19. 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 BMC Med Genet; 2014 Mar; 15():31. PubMed ID: 24606995 [TBL] [Abstract][Full Text] [Related]
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