Research of Long Qt Syndrome has been linked to Cardiac Arrhythmia, Torsades De Pointes, Sudden Cardiac Death, Tachycardia, Ventricular, Sudden Death. The study of Long Qt Syndrome has been mentioned in research publications which can be found using our bioinformatics tool below. Researched pathways related to Long Qt Syndrome include Pathogenesis, Cardiac Conduction, Localization, Innervation, Transport. These pathways complement our catalog of research reagents for the study of Long Qt Syndrome including antibodies and ELISA kits against KCNH2, KCNQ1, SCN5A, KCNE1, KCNH6.
Long Qt Syndrome Bioinformatics Tool
Laverne is a handy bioinformatics tool to help facilitate scientific exploration of related genes, diseases and pathways based on co-citations. Explore more on Long Qt Syndrome below!
For more information on how to use Laverne, please read the How to Guide.
We have 520 products for the study of Long Qt Syndrome that can be applied to Chromatin Immunoprecipitation, Western Blot, Flow Cytometry, Immunocytochemistry/Immunofluorescence, Immunohistochemistry from our catalog of antibodies and ELISA kits.
Long Qt Syndrome is also known as long qt syndrome, romano-ward syndrome, long qt syndrome, autosomal dominant, romano-ward syndrome (disorder), romano-ward long qt syndrome, long q-t syndrome, lqt.
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