Analysis of the human KCNH2(HERG) gene: Identification and characterization of a novel mutation Y667X associated with long QT syndrome and a non-pathological 9 bp insertion Communicated by: Mark H. Paalman Online Citation: Human Mutation, Mutation in Brief #325 (2000) Online http://journals.wiley.com/1059-7794/pdf/mutation/325.pdf [PDF]
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Correlation of genetic etiology with response to β-adrenergic blockade among symptomatic patients with familial long-QT syndrome [PDF]
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Chronic pentamidine aerosol prophylaxis does not induce QT-prolongation and vetricular arrythmias [PDF]
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Phase 2 Early Afterdepolarization as a Trigger of Polymorphic Ventricular Tachycardia in Acquired Long-QT Syndrome [PDF]
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Homozygous SCN5A Mutation in Long-QT Syndrome With Functional Two-to-One Atrioventricular Block [PDF]
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Long-QT Syndrome-Associated Missense Mutations in the Pore Helix of the HERG Potassium Channel [PDF]
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