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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Detalles Bibliográficos
Autores principales: Smith, Jennifer L., Anderson, Corey L., Burgess, Don E., Elayi, Claude S., January, Craig T., Delisle, Brian P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2016
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5063260/
https://www.ncbi.nlm.nih.gov/pubmed/27761161
http://dx.doi.org/10.1016/j.joa.2015.11.009

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5063260/
https://www.ncbi.nlm.nih.gov/pubmed/27761161
http://dx.doi.org/10.1016/j.joa.2015.11.009

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