APA citiranje

Bagnall, R. D., Molloy, L. K., Kalman, J. M., & Semsarian, C. (2014). Exome sequencing identifies a mutation in the ACTN2 gene in a family with idiopathic ventricular fibrillation, left ventricular noncompaction, and sudden death. BMC Med Genet.

Citação norma Chicago

Bagnall, Richard D., Laura K. Molloy, Jonathan M. Kalman, and Christopher Semsarian. "Exome Sequencing Identifies a Mutation in the ACTN2 Gene in a Family With Idiopathic Ventricular Fibrillation, Left Ventricular Noncompaction, and Sudden Death." BMC Med Genet 2014.

MLA citiranje

Bagnall, Richard D., Laura K. Molloy, Jonathan M. Kalman, and Christopher Semsarian. "Exome Sequencing Identifies a Mutation in the ACTN2 Gene in a Family With Idiopathic Ventricular Fibrillation, Left Ventricular Noncompaction, and Sudden Death." BMC Med Genet 2014.