HCN4 mutations in multiple families with bradycardia and left ventricular noncompaction cardiomyopathy

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Keywords	exome sequencing, genetics, HCN4, ion channel, left ventricular noncompaction cardiomyopathy, sinus bradycardia
Persistent URL	doi.org/10.1016/j.jacc.2014.05.045, hdl.handle.net/1765/92053
Journal	Journal of the American College of Cardiology
Organisation	Erasmus MC: University Medical Center Rotterdam
Citation APA APA Style APA-ALL Style AAA Style Cell Style Chicago Style Harvard Style IEEE Style MLA Style Nature Style Vancouver Style American-Institute-of-Physics Style Council-of-Science-Editors Style BibTex Format Endnote Format RIS Format CSL Format DOIs only Format	Milano, A., Vermeer, A., Lodder, E. M., Barc, J., Verkerk, A., Postma, A., van der Bilt, I., Baars, M., Van Haelst, P. L., Caliskan, K., Hoedemaekers, Y., Le Scouarnec, S., Redon, R., Pinto, Y., Christiaans, I., Wilde, A.& Bezzina, C. (2014). HCN4 mutations in multiple families with bradycardia and left ventricular noncompaction cardiomyopathy. Journal of the American College of Cardiology, 64(8), 745–756.https://doi.org/10.1016/j.jacc.2014.05.045

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