Mutational analysis of compound heterozygous mutation p.Q6X/p.H232R in SRD5A2 causing 46,XY disorder of sex development

MLA

Liwei Li, et al. “Mutational Analysis of Compound Heterozygous Mutation p.Q6X/p.H232R in SRD5A2 Causing 46,XY Disorder of Sex Development.” Italian Journal of Pediatrics, vol. 48, no. 1, Mar. 2022, pp. 1–13. EBSCOhost, https://doi.org/10.1186/s13052-022-01243-4.

APA

Liwei Li, Junhong Zhang, Qing Li, Li Qiao, Pengcheng Li, Yi Cui, Shujun Li, Shirui Hao, Tongqian Wu, Lili Liu, Jianmin Yin, Pingsheng Hu, Xiaowei Dou, Shuping Li, & Hui Yang. (2022). Mutational analysis of compound heterozygous mutation p.Q6X/p.H232R in SRD5A2 causing 46,XY disorder of sex development. Italian Journal of Pediatrics, 48(1), 1–13. https://doi.org/10.1186/s13052-022-01243-4

Chicago

Liwei Li, Junhong Zhang, Qing Li, Li Qiao, Pengcheng Li, Yi Cui, Shujun Li, et al. 2022. “Mutational Analysis of Compound Heterozygous Mutation p.Q6X/p.H232R in SRD5A2 Causing 46,XY Disorder of Sex Development.” Italian Journal of Pediatrics 48 (1): 1–13. doi:10.1186/s13052-022-01243-4.