APA (7th ed.) Citation

TM, P., D, A., F, B., P, M., PF, C., JK, T., . . . C, T. (2011). Whole-exome sequencing identifies homozygous AFG3L2 mutations in a spastic ataxia-neuropathy syndrome linked to mitochondrial m-AAA proteases. PLoS genetics, 7(10), e1002325. https://doi.org/10.1371/journal.pgen.1002325

Chicago Style (17th ed.) Citation

TM, Pierson, et al. "Whole-exome Sequencing Identifies Homozygous AFG3L2 Mutations in a Spastic Ataxia-neuropathy Syndrome Linked to Mitochondrial M-AAA Proteases." PLoS Genetics 7, no. 10 (2011): e1002325. https://doi.org/10.1371/journal.pgen.1002325.

MLA (9th ed.) Citation

TM, Pierson, et al. "Whole-exome Sequencing Identifies Homozygous AFG3L2 Mutations in a Spastic Ataxia-neuropathy Syndrome Linked to Mitochondrial M-AAA Proteases." PLoS Genetics, vol. 7, no. 10, 2011, p. e1002325, https://doi.org/10.1371/journal.pgen.1002325.