Functional Identification of Compound Heterozygous Mutations in the CYP17A1 Gene Resulting in Combined 17α-Hydroxylase/17,20-Lyase Deficiency
Eun Yeong Mo (Mo EY), Ji-young Lee (Lee Jy), Su Yeon Kim (Kim SY), Min Ji Kim (Kim MJ), Eun Sook Kim (Kim ES), Seungok Lee (Lee S), Je Ho Han (Han JH), Sung-dae Moon (Moon Sd)
Endocrinol Metab. 2018;33(3):413-422.   Published online 2018 Sep 18     DOI: https://doi.org/10.3803/EnM.2018.33.3.413
Citations to this article as recorded by Crossref logo
Novel mutations of the CYP17A1 gene in four Chinese 46,XX cases with partial 17a-hydroxylase/17,20-lyase deficiency
Yanjie Xia, Panlai Shi, Junke Xia, Huijuan Zhang, Lijun Xu, Xiangdong Kong
Steroids.2021; 173: 108873.     CrossRef