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A single hERG mutation underlying a spectrum of acquired and congenital long QT syndrome phenotypes

✍ Scribed by J.B. Saenen; A.D.C. Paulussen; R.J. Jongbloed; C.L. Marcelis; R.A.H.J. Gilissen; J. Aerssens; D.J. Snyders; A.L. Raes

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