Publications
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Filtres: Author is Wang, Jou-Kou [Enlever les filtres]
« 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, p. 1295-304, 2012.
, « 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, p. 268-78, 2004.
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