Inleiding
In dit hoofdstuk wordt stilgestaan bij de genetische aspecten van AHA. Het is een veld dat sterk in beweging is en tabellen met genen die een rol spelen bij het ontstaan van hartafwijkingen zijn waarschijnlijk bij het ter perse gaan van dit boek alweer verouderd. Toch proberen we een aantal algemene principes uiteen te zetten en completeren we dit hoofdstuk met een lijst definities van genetische begrippen en technieken, in de hoop dat dit het lezen van dit hoofdstuk en ook van verdere literatuur op dit gebied vergemakkelijkt.
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Literatuur
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Websites
Genereviews: www.ncbi.nlm.nih.gov/sites/GeneTests.
Database of genomic variants: http://projects.tcag.ca/variation.
Online mendelian inheritance in man: www.ncbi.nlm.nih.gov/omim.
University of California Santa Cruz Genome browser: http://genome.ucsc.edu.
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Kerstjens-Frederikse, W., Hofstra, R. (2013). Genetische aspecten van aangeboren hartafwijkingen. In: Mulder, B., Pieper, P., Meijboom, F., Hamer, J. (eds) Aangeboren hartafwijkingen bij volwassenen. Bohn Stafleu van Loghum, Houten. https://doi.org/10.1007/978-90-368-0307-6_23
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DOI: https://doi.org/10.1007/978-90-368-0307-6_23
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