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Publications by Giulia Frisso
Novel Deletion Mutation in the Cardiac Sodium Channel Inactivation Gate Causes Long QT Syndrome
International Journal of Cardiology
Cardiovascular Medicine
Cardiology
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Novel Arrhythmogenic Mechanism Revealed by a Long-Qt Syndrome Mutation in the Cardiac Na+ Channel
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Congenital Long-Qt Syndrome Caused by a Novel Mutation in a Conserved Acidic Domain of the Cardiac Na+ Channel
Circulation
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Mutation of an A-Kinase-Anchoring Protein Causes Long-Qt Syndrome
Proceedings of the National Academy of Sciences of the United States of America
Multidisciplinary
Novel Mutation in the Per-Arnt-Sim Domain of KCNH2 Causes a Malignant Form of Long-Qt Syndrome
Circulation
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Congenital Long QT Syndrome of Particularly Malignant Course Connected With So Far Unknown Mutation in the Sodium Channel SCN5A Gene
Cardiology Journal
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hERG Channel Trafficking: Novel Targets in Drug-Induced Long QT Syndrome
Biochemical Society Transactions
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R231C Mutation in KCNQ1 Causes Long QT Syndrome Type 1 and Familial Atrial Fibrillation
Heart Rhythm
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FGF12A Counteracts Long Qt Syndrome-Linked Inactivation Deficiency
Biophysical Journal
Biophysics
Ion Channel Mechanisms Related to Sudden Cardiac Death in Phenotype-Negative Long-Qt Syndrome Genotype-Phenotype Correlations of the KCNQ1(S349W) Mutation
Journal of Cardiovascular Electrophysiology
Cardiovascular Medicine
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