Novel Calmodulin Mutations Associated with Congenital Long QT Syndrome Affect Calcium Current in Human Cardiomyocytes

BACKGROUND: Calmodulin (CaM) mutations are associated with cardiac arrhythmia susceptibility including the congenital long QT syndrome (LQTS). OBJECTIVE: To determine the clinical, genetic and functional features of two novel CaM mutations in children with life-threatening ventricular arrhythmias. M...

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Bibliografiska uppgifter
I publikationen:Heart Rhythm
Huvudupphovsmän: Pipilas, Daniel C., Johnson, Christopher N., Webster, Gregory, Schlaepfer, Jurg, Fellmann, Florence, Sekarski, Nicole, Wren, Lisa M., Ogorodnik, Kateryna V., Chazin, Daniel M., Chazin, Walter J., Crotti, Lia, Bhuiyan, Zahurul A., George, Alfred L.
Materialtyp: Artigo
Språk:Inglês
Publicerad: 2016
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Article
Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC5035189/
https://ncbi.nlm.nih.gov/pubmed/27374306
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.hrthm.2016.06.038
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