APA (7th ed.) Citation

Grošelj, U., Tanšek, M. Ž., Podkrajšek, K. T., Hovnik, T., Battelino, T., & Dolžan, V. (2016). Clinical Role of CYP2C19 Polymorphisms in Patients with Congenital Adrenal Hyperplasia Due to 21-hydroxylase Deficiency. Acta Chimica Slovenica, 63(1), 33. https://doi.org/10.17344/acsi.2015.1797

Chicago Style (17th ed.) Citation

Grošelj, Urh, Mojca Žerjav Tanšek, Katarina Trebušak Podkrajšek, Tinka Hovnik, Tadej Battelino, and Vita Dolžan. "Clinical Role of CYP2C19 Polymorphisms in Patients with Congenital Adrenal Hyperplasia Due to 21-hydroxylase Deficiency." Acta Chimica Slovenica 63, no. 1 (2016): 33. https://doi.org/10.17344/acsi.2015.1797.

MLA (9th ed.) Citation

Grošelj, Urh, et al. "Clinical Role of CYP2C19 Polymorphisms in Patients with Congenital Adrenal Hyperplasia Due to 21-hydroxylase Deficiency." Acta Chimica Slovenica, vol. 63, no. 1, 2016, p. 33, https://doi.org/10.17344/acsi.2015.1797.