Homozygous SCN5A Mutation in Long-QT Syndrome With Functional Two-to-One Atrioventricular Block [PDF]
Jean‐Marc Lupoglazoff+8 more
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Long-QT Syndrome-Associated Missense Mutations in the Pore Helix of the HERG Potassium Channel [PDF]
Fu-De Huang+4 more
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Effectiveness and Limitations of β-Blocker Therapy in Congenital Long-QT Syndrome [PDF]
Robert M. Gow
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Variable Expression of Long QT Syndrome Among Gene Carriers from Families with Five Different HERG Mutations [PDF]
Jesaia Benhorin+11 more
openalex +1 more source
Drug-induced long QT syndrome: Assessment by the in vivo canine model.
Atsushi Sugiyama+2 more
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Inherited Brugada and Long QT-3 Syndrome Mutations of a Single Residue of the Cardiac Sodium Channel Confer Distinct Channel and Clinical Phenotypes [PDF]
Ilaria Rivolta+8 more
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A founder mutation of the potassium channel KCNQ1 in long QT syndrome
Kirsi Piippo+7 more
openalex +1 more source
Dynamic analysis of the QT interval in long QT1 syndrome patients with a normal phenotype [PDF]
Gilles Lande
openalex +1 more source