Genetic basis of cardiac ion channel diseases

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Query: faculty: "AMC-UvA" and publication year: "2008"

Author	T. T. Koopmann
Title	Genetic basis of cardiac ion channel diseases
Promotors	A.A.M Wilde, A.F.M. Moorman
Co-promotor	C.R. Bezzina
Date	17-06-2008
Year	2008
Pages	172
ISBN	978-90-9023108-2
Faculty	AMC-UvA
Keywords	Cardiovascular diseases, Arrhythmias, Ion channels, Hereditary disposition
Classification	44.85 cardiology
Language	English
Document type	Dissertation
Download papers	Thesis Cover Contents Chapter 1: Introduction. Ion channels involved in genetic cardiac arrhythmias Chapter 2: Voltage-gated sodium channels: action players with many faces Chapter 3: A mutation in the human cardiac sodium channel (E161K) contributes to sick sinus syndrome, conduction disease and Brugada syndrome in two families Chapter 4: A common sodium channel promoter haplotype in Asian subjects underlies variability in cardiac conduction Chapter 5: Polymorphisms in the cardiac sodium channel promoter displaying variant in vitro expression activity Chapter 6: Sodium channel β1-subunit mutations associated with Brugada syndrome and cardiac conduction disease Chapter 7: Exclusion of multiple candidate genes and large genomic rearrangements in SCN5A in a Dutch Brugada syndrome cohort 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 The intrinsic complexity and future perspectives of genetic research Summary / Samenvatting Dankwoord List of publications
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