AKAP9 is a Genetic Modifier of Congenital Long-QT Syndrome Type 1

BACKGROUND: Long-QT syndrome (LQTS), a cardiac arrhythmia disorder with variable phenotype, often results in devastating outcomes including sudden cardiac death. Variable expression, independently from the primary disease-causing mutation, can partly be explained by genetic modifiers. This study inv...

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Bibliographic Details
Published in:Circ Cardiovasc Genet
Main Authors: de Villiers, Carin P., van der Merwe, Lize, Crotti, Lia, Goosen, Althea, George, Alfred L., Schwartz, Peter J., Brink, Paul A., Moolman-Smook, Johanna C., Corfield, Valerie A.
Format: Artigo
Language:Inglês
Published: 2014
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Article
Online Access:https://ncbi.nlm.nih.gov/pmc/articles/PMC4270884/
https://ncbi.nlm.nih.gov/pubmed/25087618
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1161/CIRCGENETICS.113.000580
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