APA (7th ed.) Citation

P, V., R, N., A, H., MA, F., NH, S., C, G., . . . DF, N. (2015). Exome sequencing in an admixed isolated population indicates NFXL1 variants confer a risk for specific language impairment. PLoS genetics, 11(3), e1004925. https://doi.org/10.1371/journal.pgen.1004925

Chicago Style (17th ed.) Citation

P, Villanueva, et al. "Exome Sequencing in an Admixed Isolated Population Indicates NFXL1 Variants Confer a Risk for Specific Language Impairment." PLoS Genetics 11, no. 3 (2015): e1004925. https://doi.org/10.1371/journal.pgen.1004925.

MLA (9th ed.) Citation

P, Villanueva, et al. "Exome Sequencing in an Admixed Isolated Population Indicates NFXL1 Variants Confer a Risk for Specific Language Impairment." PLoS Genetics, vol. 11, no. 3, 2015, p. e1004925, https://doi.org/10.1371/journal.pgen.1004925.