Targeted long-read sequencing identifies missing pathogenic variant in unsolved 11β-hydroxylase deficiency.

MLA

Liu, Jidong, et al. “Targeted Long-Read Sequencing Identifies Missing Pathogenic Variant in Unsolved 11β-Hydroxylase Deficiency.” BMC Endocrine Disorders, vol. 24, no. 1, Oct. 2024, pp. 1–8. EBSCOhost, https://doi.org/10.1186/s12902-024-01748-5.

APA

Liu, J., Tian, H., Jin, X., Wang, Y., Zhang, Z., Li, M., Dai, L., Zhang, X., & Jiang, L. (2024). Targeted long-read sequencing identifies missing pathogenic variant in unsolved 11β-hydroxylase deficiency. BMC Endocrine Disorders, 24(1), 1–8. https://doi.org/10.1186/s12902-024-01748-5

Chicago

Liu, Jidong, Huihui Tian, Xinchen Jin, Yanxiang Wang, Zhenhong Zhang, Mengxue Li, Lulu Dai, Xiaoli Zhang, and Ling Jiang. 2024. “Targeted Long-Read Sequencing Identifies Missing Pathogenic Variant in Unsolved 11β-Hydroxylase Deficiency.” BMC Endocrine Disorders 24 (1): 1–8. doi:10.1186/s12902-024-01748-5.