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Genetic basis of cardiac ion channel diseases
Koopmann, T.
Publication date
2008
Link to publication
Citation for published version (APA):
Koopmann, T. (2008). Genetic basis of cardiac ion channel diseases.
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CONTENTS
Chapter 1 Introduction
Ion channels involved in genetic cardiac arrhythmias.
To be published in part as bookchapter in: “Ion channels biophysics and diseases” (published by research signpost) Chapter 2 Voltage-gated sodium channels: action players with many
faces.
Annals of medicine. 2006;38(7):472-82.
Chapter 3 A mutation in the human cardiac sodium channel (E161K) contributes to sick sinus syndrome, conduction disease and Brugada syndrome in two families.
Journal of molecular and cellular cardiology. 2005;38:969-81. Chapter 4 A common sodium channel promoter haplotype in Asian
subjects underlies variability in cardiac conduction.
Circulation. 2006;113(3):338-44.
Chapter 5 Polymorphisms in the cardiac sodium channel promoter displaying variant in vitro expression activity.
European journal of human genetics. 2008;16(3):350-7.
Chapter 6 Sodium channel ββ1-subunit mutations associated with Brugada syndrome and cardiac conduction disease.
The journal of clinical investigation.In press
Chapter 7 Exclusion of multiple candidate genes and large genomic rearrangements in SCN5A in a Dutch Brugada syndrome cohort.
Heart rhythm. 2007;4(6):752-5.
Chapter 8 Long QT Syndrome caused by a large duplication in the KCNH2 (HERG) gene undetectable by the PCR-based exon-scanning methodologies employed to date.
Heart rhythm. 2006;3(1):52-5.
The intrinsic complexity and future perspectives of genetic research Summary / Samenvatting Dankwoord List of publications CONTENTS 7 9 37 57 79 95 109 131 141 149 157 165 169
GENETICBASIS OFCARDIACIONCHANNELDISEASES
