Spectrum and prevalence of mutations from the first 2,500 consecutive unrelated patients referred for the FAMILION long QT syndrome genetic test.

MLA

Kapplinger, Jamie D., et al. “Spectrum and Prevalence of Mutations from the First 2,500 Consecutive Unrelated Patients Referred for the FAMILION Long QT Syndrome Genetic Test.” Heart Rhythm, vol. 6, no. 9, Sept. 2009, pp. 1297–303. EBSCOhost, https://doi.org/10.1016/j.hrthm.2009.05.021.

APA

Kapplinger, J. D., Tester, D. J., Salisbury, B. A., Carr, J. L., Harris-Kerr, C., Pollevick, G. D., Wilde, A. A. M., & Ackerman, M. J. (2009). Spectrum and prevalence of mutations from the first 2,500 consecutive unrelated patients referred for the FAMILION long QT syndrome genetic test. Heart Rhythm, 6(9), 1297–1303. https://doi.org/10.1016/j.hrthm.2009.05.021

Chicago

Kapplinger, Jamie D, David J Tester, Benjamin A Salisbury, Janet L Carr, Carole Harris-Kerr, Guido D Pollevick, Arthur A M Wilde, and Michael J Ackerman. 2009. “Spectrum and Prevalence of Mutations from the First 2,500 Consecutive Unrelated Patients Referred for the FAMILION Long QT Syndrome Genetic Test.” Heart Rhythm 6 (9): 1297–1303. doi:10.1016/j.hrthm.2009.05.021.