APA (7th ed.) Citation

Bilgüvar, K., Öztürk, A. K., Louvi, A., Kwan, K. Y., Choi, M., Tatlı, B., . . . Günel, M. (2010). Whole-exome sequencing identifies recessive WDR62 mutations in severe brain malformations. Nature (London), 467(7312), 207-210. https://doi.org/10.1038/nature09327

Chicago Style (17th ed.) Citation

Bilgüvar, Kaya, et al. "Whole-exome Sequencing Identifies Recessive WDR62 Mutations in Severe Brain Malformations." Nature (London) 467, no. 7312 (2010): 207-210. https://doi.org/10.1038/nature09327.

MLA (9th ed.) Citation

Bilgüvar, Kaya, et al. "Whole-exome Sequencing Identifies Recessive WDR62 Mutations in Severe Brain Malformations." Nature (London), vol. 467, no. 7312, 2010, pp. 207-210, https://doi.org/10.1038/nature09327.