Molecular pathogenesis of long QT syndrome type 2

The molecular mechanisms underlying congenital long QT syndrome (LQTS) are now beginning to be understood. New insights into the etiology and therapeutic strategies are emerging from heterologous expression studies of LQTS-linked mutant proteins, as well as inducible pluripotent stem cell derived ca...

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Bibliographic Details
Published in:J Arrhythm
Main Authors: Smith, Jennifer L., Anderson, Corey L., Burgess, Don E., Elayi, Claude S., January, Craig T., Delisle, Brian P.
Format: Artigo
Language:Inglês
Published: Elsevier 2016
Subjects:
Review
Online Access:https://ncbi.nlm.nih.gov/pmc/articles/PMC5063260/
https://ncbi.nlm.nih.gov/pubmed/27761161
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.joa.2015.11.009
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