APA (7th ed.) Citation

Johnson, S. R., Leo, P. J., McInerney‐Leo, A. M., Anderson, L. K., Marshall, M., McGown, I., . . . Duncan, E. L. (2018). Whole‐exome sequencing for mutation detection in pediatric disorders of insulin secretion: Maturity onset diabetes of the young and congenital hyperinsulinism. Pediatric diabetes, 19(4), 656-662. https://doi.org/10.1111/pedi.12638

Chicago Style (17th ed.) Citation

Johnson, S R., et al. "Whole‐exome Sequencing for Mutation Detection in Pediatric Disorders of Insulin Secretion: Maturity Onset Diabetes of the Young and Congenital Hyperinsulinism." Pediatric Diabetes 19, no. 4 (2018): 656-662. https://doi.org/10.1111/pedi.12638.

MLA (9th ed.) Citation

Johnson, S R., et al. "Whole‐exome Sequencing for Mutation Detection in Pediatric Disorders of Insulin Secretion: Maturity Onset Diabetes of the Young and Congenital Hyperinsulinism." Pediatric Diabetes, vol. 19, no. 4, 2018, pp. 656-662, https://doi.org/10.1111/pedi.12638.