Publications
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Filters: Author is Wu, Mei-Hwan [Clear All Filters]
, “Coexisting mutations/polymorphisms of the long QT syndrome genes in patients with repaired Tetralogy of Fallot are associated with the risks of life-threatening events.”, Hum Genet, vol. 131, no. 8, pp. 1295-304, 2012.
, “In utero onset of long QT syndrome with atrioventricular block and spontaneous or lidocaine-induced ventricular tachycardia: compound effects of hERG pore region mutation and SCN5A N-terminus variant.”, Heart Rhythm, vol. 5, no. 11, pp. 1567-74, 2008.
, “A novel SCN5A mutation manifests as a malignant form of long QT syndrome with perinatal onset of tachycardia/bradycardia.”, Cardiovasc Res, vol. 64, no. 2, pp. 268-78, 2004.
