APA (7th ed.) Citation

Rubtsov, P., Nizhnik, A., Dedov, I., Kalinchenko, N., Petrov, V., Orekhova, A., . . . Tiulpakov, A. (2015). Partial deficiency of 17γ-hydroxylase/17,20-lyase caused by a novel missense mutation in the canonical cytochrome heme-interacting motif. European Journal of Endocrinology, 172(5), K19. https://doi.org/10.1530/EJE-14-0834

Chicago Style (17th ed.) Citation

Rubtsov, Petr, Alexander Nizhnik, Ivan Dedov, Natalia Kalinchenko, Vasily Petrov, Anna Orekhova, Pavel Spirin, Vladimir Prassolov, and Anatoly Tiulpakov. "Partial Deficiency of 17γ-hydroxylase/17,20-lyase Caused by a Novel Missense Mutation in the Canonical Cytochrome Heme-interacting Motif." European Journal of Endocrinology 172, no. 5 (2015): K19. https://doi.org/10.1530/EJE-14-0834.

MLA (9th ed.) Citation

Rubtsov, Petr, et al. "Partial Deficiency of 17γ-hydroxylase/17,20-lyase Caused by a Novel Missense Mutation in the Canonical Cytochrome Heme-interacting Motif." European Journal of Endocrinology, vol. 172, no. 5, 2015, p. K19, https://doi.org/10.1530/EJE-14-0834.