APA (7th ed.) Citation

Fujita, A., Tsukaguchi, H., Koshimizu, E., Nakazato, H., Itoh, K., Kuraoka, S., . . . Miyake, N. (2018). Homozygous splicing mutation in NUP133 causes Galloway–Mowat syndrome. Annals of neurology, 84(6), 814-828. https://doi.org/10.1002/ana.25370

Chicago Style (17th ed.) Citation

Fujita, Atsushi, et al. "Homozygous Splicing Mutation in NUP133 Causes Galloway–Mowat Syndrome." Annals of Neurology 84, no. 6 (2018): 814-828. https://doi.org/10.1002/ana.25370.

MLA (9th ed.) Citation

Fujita, Atsushi, et al. "Homozygous Splicing Mutation in NUP133 Causes Galloway–Mowat Syndrome." Annals of Neurology, vol. 84, no. 6, 2018, pp. 814-828, https://doi.org/10.1002/ana.25370.