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Publications by Yung R Lau

Clinical, Genetic, and Biophysical Characterization of a Homozygous HERG Mutation Causing Severe Neonatal Long QT Syndrome

Pediatric Research

English

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Physiological Properties of hERG 1a/1b Heteromeric Currents and a hERG 1b-Specific Mutation Associated With Long-Qt Syndrome

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Late-Onset Severe Long QT Syndrome

Annals of Noninvasive Electrocardiology

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Clinical and Electrophysiological Characterization of a Novel Mutation (F193L) in the KCNQ1 Gene Associated With Long QT Syndrome

Clinical Science

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hERG Channel Trafficking: Novel Targets in Drug-Induced Long QT Syndrome

Biochemical Society Transactions

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A Novel Germline CDKN1B Mutation Causing Multiple Endocrine Tumors: Clinical, Genetic and Functional Characterization

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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

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Novel Characteristics of a Trafficking-Defective G572r-hERG Channel Linked to Hereditary Long QT Syndrome

Canadian Journal of Cardiology

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Non Genetic Risk Factors of Long-Qt Syndrome

Open Journal of Genetics

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Pediatric Cohort With Long QT Syndrome – KCNH2 Mutation Carriers Present Late Onset but Severe Symptoms –

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