Yuan, X., Lu, L., Chen, S., Jiang, J., Wang, X., Liu, Z., . . . Lu, Z. (2018). A Chinese patient with 11β-hydroxylase deficiency due to novel compound heterozygous mutation in CYP11B1 gene: A case report. BMC Endocr Disord.
Citação norma ChicagoYuan, Xianxian, Lin Lu, Shi Chen, Jun Jiang, Xiangqing Wang, Zhihui Liu, Huijuan Zhu, Hui Pan, and Zhaolin Lu. "A Chinese Patient With 11β-hydroxylase Deficiency Due to Novel Compound Heterozygous Mutation in CYP11B1 Gene: A Case Report." BMC Endocr Disord 2018.
Citação norma MLAYuan, Xianxian, et al. "A Chinese Patient With 11β-hydroxylase Deficiency Due to Novel Compound Heterozygous Mutation in CYP11B1 Gene: A Case Report." BMC Endocr Disord 2018.
Nota: a formatação da citação pode não corresponder 100% ao definido pela respectiva norma.