Nakano, K., Kubota, Y., Mori, T., Chiga, M., Mori, T., Sonoda, S., . . . Kubota, A. (2020). Familial cases of pseudohypoaldosteronism type II harboring a novel mutation in the Cullin 3 gene. Nephrology, 25(11), 818. https://doi.org/10.1111/nep.13752
Chicago Style (17th ed.) CitationNakano, Kiyoshi, et al. "Familial Cases of Pseudohypoaldosteronism Type II Harboring a Novel Mutation in the Cullin 3 Gene." Nephrology 25, no. 11 (2020): 818. https://doi.org/10.1111/nep.13752.
MLA (9th ed.) CitationNakano, Kiyoshi, et al. "Familial Cases of Pseudohypoaldosteronism Type II Harboring a Novel Mutation in the Cullin 3 Gene." Nephrology, vol. 25, no. 11, 2020, p. 818, https://doi.org/10.1111/nep.13752.
Warning: These citations may not always be 100% accurate.