Cite

    Liu, Y., Zheng, J., Liu, N., Xu, X., Zhang, X., Zhang, Y., Li, G., Liu, G., Cai, C., & Shu, J. (2020). the spectrum of CYP21A2 gene mutations in patients with classic salt wasting form of 2l‐hydroxylase deficiency in a Chinese cohort. Molecular genetics & genomic medicine, 8(11), n/a. http://access.bl.uk/ark:/81055/vdc_100120109360.0x000008