Two cases of 17α-hydroxylase/17,20-lyase deficiency caused by the CYP17A1 mutation
Hae In Lee, Ahreum Kwon, Jung Hwan Suh, Han Saem Choi, Kyung Chul Song, Hyun Wook Chae, Ho-Seong Kim
Ann Pediatr Endocrinol Metab. 2021;26(1):66-70.   Published online 2021 Mar 31     DOI: https://doi.org/10.6065/apem.2040184.092
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