APA (7th ed.) Citation

Salfati, E. L., Spencer, E. G., Topol, S. E., Muse, E. D., Rueda, M., Lucas, J. R., . . . Torkamani, A. (2019). Re-analysis of whole-exome sequencing data uncovers novel diagnostic variants and improves molecular diagnostic yields for sudden death and idiopathic diseases. Genome Medicine, 11(1), 1. https://doi.org/10.1186/s13073-019-0702-2

Chicago Style (17th ed.) Citation

Salfati, Elias L., et al. "Re-analysis of Whole-exome Sequencing Data Uncovers Novel Diagnostic Variants and Improves Molecular Diagnostic Yields for Sudden Death and Idiopathic Diseases." Genome Medicine 11, no. 1 (2019): 1. https://doi.org/10.1186/s13073-019-0702-2.

MLA (9th ed.) Citation

Salfati, Elias L., et al. "Re-analysis of Whole-exome Sequencing Data Uncovers Novel Diagnostic Variants and Improves Molecular Diagnostic Yields for Sudden Death and Idiopathic Diseases." Genome Medicine, vol. 11, no. 1, 2019, p. 1, https://doi.org/10.1186/s13073-019-0702-2.