Multiplex ligation-dependent probe amplification copy number variant analysis in patients with acquired long QT syndrome - Williams, Victoria S.; Cresswell, Carl J.; Ruspi, Gerhard; Yang, Tao; Atak, Thomas C.; McLoughlin, Matthew; Ingram, Christiana D.; Ramirez, Andrea H.; Roden, Dan; Armstrong, Martin (Europace (London, England), 2015)
Keywords: Adult; DNA Copy Number Variations - genetics; Female; Genetic Markers - genetics; Genetic Predisposition to Disease - epidemiology; Genetic Predisposition to Disease - genetics; Humans; Long QT Syndrome - diagnosis; Long QT Syndrome - epidemiology; Long QT Syndrome - genetics; Male; Multiplex Polymerase Chain Reaction; Mutation - genetics; Polymorphism, Single Nucleotide - genetics; Potassium Channels - genetics; Prevalence; Risk Factors; United Kingdom - epidemiology; Long QT syndrome; Copy number variation; Multiplex ligation-dependent probe amplification; MLPA; Genes