Diagnosis of mitochondrial disorders by concomitant next-generation sequencing of the exome and mitochondrial genome

MLA

Darrell L. Dinwiddie, et al. “Diagnosis of Mitochondrial Disorders by Concomitant Next-Generation Sequencing of the Exome and Mitochondrial Genome.” Genomics, vol. 102, Sept. 2013, pp. 148–56. EBSCOhost, https://doi.org/10.1016/j.ygeno.2013.04.013.

APA

Darrell L. Dinwiddie, Stephen F. Kingsmore, Carol J. Saunders, Emily G. Farrow, Laurie D. Smith, Andrea M. Atherton, Meghan Strenk, Neil A. Miller, & Sarah E Soden. (2013). Diagnosis of mitochondrial disorders by concomitant next-generation sequencing of the exome and mitochondrial genome. Genomics, 102, 148–156. https://doi.org/10.1016/j.ygeno.2013.04.013

Chicago

Darrell L. Dinwiddie, Stephen F. Kingsmore, Carol J. Saunders, Emily G. Farrow, Laurie D. Smith, Andrea M. Atherton, Meghan Strenk, Neil A. Miller, and Sarah E Soden. 2013. “Diagnosis of Mitochondrial Disorders by Concomitant Next-Generation Sequencing of the Exome and Mitochondrial Genome.” Genomics 102 (September): 148–56. doi:10.1016/j.ygeno.2013.04.013.