Lee, H. I., Kwon, A., Suh, J. H., Choi, H. S., Song, K. C., Chae, H. W., & Kim, H. (2021). Two cases of 17α-hydroxylase/17,20-lyase deficiency caused by the CYP17A1 mutation. Ann Pediatr Endocrinol Metab.
Citação norma ChicagoLee, Hae In, Ahreum Kwon, Jung Hwan Suh, Han Saem Choi, Kyung Chul Song, Hyun Wook Chae, and Ho-Seong Kim. "Two Cases of 17α-hydroxylase/17,20-lyase Deficiency Caused By the CYP17A1 Mutation." Ann Pediatr Endocrinol Metab 2021.
Citação norma MLALee, Hae In, et al. "Two Cases of 17α-hydroxylase/17,20-lyase Deficiency Caused By the CYP17A1 Mutation." Ann Pediatr Endocrinol Metab 2021.
Nota: a formatação da citação pode não corresponder 100% ao definido pela respectiva norma.